objective resume for pharmaceutical

Terms And Conditions
Privacy Policy
Editorial Policy

Home » 143+ Pharmacist Resume Objective For Impactful Job Applications

143+ Pharmacist Resume Objective For Impactful Job Applications

Are you ready to take your pharmacy career to the next level? Crafting a compelling resume objective is the first step to landing your dream job in the pharmaceutical world. In this blog post, we’ll delve into the art of writing a standout pharmacist resume objective that will make you a top contender in the job market.

Whether you’re a seasoned pharmacist or just starting out in the field, these tips and examples will help you create a resume objective that sets you apart. Get ready to revamp your resume and set yourself up for success in the competitive pharmacy industry!

Table of Contents

What To Include In Pharmacist Resume Objective

Position-specific : Clearly state your desired role in the pharmaceutical field.
Skills showcase : Highlight relevant skills such as medication management and patient care.
Career goals : Express your aspirations within the pharmacy profession.
Value proposition : Communicate how you can contribute to the employer’s success.
Tailored approach : Customize the objective for each job application

Career Objective for Resume For Fresher in Pharmacy:

Seeking to apply my pharmaceutical knowledge to provide exceptional patient care.
Eager to learn and grow as a pharmacy professional in a dynamic work environment.
Aspiring to contribute my skills to a pharmacy team dedicated to improving health outcomes.
Seeking an entry-level position to kick-start my career in the pharmaceutical industry.
Passionate about utilizing my education to make a positive impact in the pharmacy field.
Seeking a challenging role to develop my skills and knowledge in pharmaceutical practice.
Looking for an opportunity to apply my academic learning in a practical pharmacy setting.
Aspiring to contribute to a pharmacy team with a focus on delivering quality care.
Seeking a position that allows me to learn and grow while making a difference in patient lives.
Eager to leverage my education to support pharmacy operations and patient well-being.
115+ Catchy Career Objective for Doctors ideas & Examples
101+ Catchy Career Objective for Nursing Student ideas list
133+ Unique Career Objective for MBA Freshers ideas & Examples

Career Objective For Pharmacist:

Dedicated pharmacist aiming to optimize medication therapy and patient outcomes.
Seeking a pharmacist position to utilize my expertise in medication management.
Pharmacist committed to delivering exceptional pharmaceutical care and counseling.
Aspiring to lead pharmacy operations and enhance medication safety and efficacy.
Experienced pharmacist dedicated to providing personalized care and improving health outcomes.
Seeking a pharmacist role to apply my clinical knowledge and expertise in patient care.
Pharmacist passionate about optimizing drug therapy and promoting wellness.
Committed to ensuring the safe and effective use of medications as a pharmacist.
Seeking a pharmacist position to contribute to a collaborative healthcare team.
Pharmacist with a focus on delivering high-quality pharmaceutical services and education.

Pharmacy Technician Resume Objective:

Detail-oriented pharmacy technician dedicated to ensuring accurate medication dispensing.
Seeking a pharmacy technician role to support efficient pharmacy operations and patient care.
Pharmacy technician committed to maintaining medication inventory and assisting pharmacists.
Eager to apply my organizational skills and pharmacy knowledge in a technician role.
Aspiring to contribute to a pharmacy team by providing exceptional customer service and support.
Pharmacy technician focused on delivering accurate and efficient medication dispensing.
Seeking a role to utilize my technical skills and contribute to a patient-centered pharmacy environment.
Dedicated pharmacy technician aiming to support pharmacy operations and medication management.
Detail-oriented individual seeking a pharmacy technician position to assist in delivering quality care.
Pharmacy technician committed to upholding pharmacy standards and ensuring patient safety.

Career Objective for Fresh Graduate Pharmacist:

Recent pharmacy graduate eager to apply clinical knowledge and skills in a professional setting.
Aspiring to begin my pharmacy career by contributing to a healthcare team focused on patient care.
Seeking an entry-level pharmacist position to develop expertise in medication management.
Fresh graduate pharmacist dedicated to providing compassionate and personalized pharmaceutical care.
Eager to apply my education and training to support pharmacy operations and patient well-being.
Recent pharmacy graduate committed to learning and growing in a dynamic pharmacy environment.
Aspiring to contribute to a pharmacy team by delivering high-quality pharmaceutical services.
Seeking an opportunity to apply my academic learning and contribute to pharmacy practice.
Fresh graduate pharmacist aiming to make a positive impact on patient health and wellness.
Committed to developing clinical skills and expertise as a new graduate pharmacist.

Pharmacist CV Objective:

Experienced pharmacist seeking a leadership role to optimize pharmacy operations and patient care.
Pharmacist with a focus on medication therapy management and interdisciplinary collaboration.
Seeking a pharmacist position to apply clinical expertise and contribute to healthcare outcomes.
Committed to delivering evidence-based pharmaceutical care and promoting medication safety.
Experienced pharmacist dedicated to mentoring and developing pharmacy staff.
Pharmacist with a focus on continuous quality improvement and patient-centered care.
Seeking a pharmacist role to lead pharmacy initiatives and enhance medication management.
Pharmacist committed to leveraging technology to improve medication safety and efficiency.
Experienced in pharmaceutical management and dedicated to optimizing pharmacy services.
Pharmacist with a focus on developing and implementing pharmacy best practices.
133+ Medical Assistant Resume Objective To Land Your Dream Job
85+ Career Objective For CSE Freshers To Propel Your Success
107+ Attractive Career Objective for NGO Resume Ideas

Catchy Pharmacist Resume Objective Statement:

Dedicated pharmacist aiming to enhance medication therapy and patient wellness.
Seeking a pharmacist position to apply clinical expertise and improve healthcare outcomes.
Pharmacist committed to delivering personalized pharmaceutical care and counseling.
Aspiring to lead pharmacy operations and optimize medication safety and efficacy.
Experienced pharmacist dedicated to ensuring the safe and effective use of medications.
Seeking a pharmacist role to provide evidence-based pharmaceutical care and promote wellness.
Pharmacist committed to leveraging technology to improve medication management and patient outcomes.

Pharmacist Resume Objective Examples:

Pharmacist dedicated to optimizing medication therapy and patient outcomes.
Seeking a pharmacist position to utilize expertise in medication management and counseling.
Committed to delivering exceptional pharmaceutical care and promoting wellness.
Pharmacist focused on delivering high-quality pharmaceutical services and education.
Seeking a pharmacist role to apply clinical knowledge and expertise in patient care.
Pharmacist committed to ensuring the safe and effective use of medications and promoting wellness.
Experienced pharmacist aiming to contribute to a collaborative healthcare team.

Career Objective for Pharmacy Freshers:

Objective for pharmacist resume:.

Pharmacist committed to optimizing medication therapy and patient wellness.
Dedicated to delivering personalized pharmaceutical care and counseling.
69+ Objective For Customer Service To Unleash Your Potential
65+ Objective for Medical Records Clerk: Key to Recognition
63+ Resume Objective for Office Clerk: Empower Your Application

Resume Objective for Pharmacy Students:

Detail-oriented pharmacy student dedicated to learning and growing in a practical setting.
Seeking a pharmacy internship to apply academic learning in a real-world pharmacy environment.
Eager to gain hands-on experience and contribute to pharmacy operations and patient care.
Aspiring to develop clinical skills and expertise to support pharmacy practice.
Pharmacy student committed to upholding pharmacy standards and ensuring patient safety.
Detail-oriented individual seeking a pharmacy internship to assist in delivering quality care.
Pharmacy student aiming to make a positive impact on patient health and wellness.
Committed to learning and growing in a dynamic pharmacy environment.
Eager to apply academic learning and contribute to pharmacy practice.
Aspiring to support pharmacy operations and patient well-being as a pharmacy student.

Career Objective for Pharma Fresher:

Aspiring to apply my pharmaceutical knowledge to provide exceptional patient care.
Eager to learn and grow as a pharmaceutical professional in a dynamic work environment.
Passionate about utilizing my education to make a positive impact in the pharma field.
Looking for an opportunity to apply my academic learning in a practical pharmaceutical setting.
Aspiring to contribute to a pharmaceutical team with a focus on delivering quality care.
Eager to leverage my education to support pharmaceutical operations and patient well-being.

Pharmacist Career Objective:

Career objective for pharmacist cv:, pharmacist objective for resume:.

Pharmacist dedicated to optimizing medication therapy and patient wellness.
75+ Best Resume Objective For Call Center To Elevate Your Career
75+ Catchy Career Objective For Fresher To Land your Dream job
91+ Dynamic Objective for Sales Resume to Catapult Your Success

Key Skills to Highlight in Pharmacist Resume Objective:

Medication Management : Showcase your ability to accurately dispense and manage medications, ensuring patient safety and well-being.
Patient Care : Highlight your dedication to providing personalized care, counseling patients on medication usage, and promoting overall wellness.
Pharmaceutical Knowledge : Emphasize your understanding of drug interactions, dosage requirements, and pharmaceutical best practices.
Interpersonal Communication : Illustrate your strong communication skills, essential for collaborating with healthcare teams and effectively engaging with patients.
Attention to Detail : Demonstrate your precision in maintaining medication records, ensuring accuracy in dispensing, and adhering to pharmacy regulations and protocols

Types Of Pharmacist Resume Objective

Career Change Objective : For professionals transitioning into pharmacy, emphasize transferable skills and express passion for the pharmaceutical field.
Entry-Level Objective : Tailored for recent graduates or individuals with limited experience, focus on eagerness to learn, contribute, and grow within a pharmacy setting.
Experienced Pharmacist Objective : Highlight years of experience, leadership capabilities, and a track record of improving patient care and pharmacy operations.
Pharmacy Internship Objective : Geared towards students or new graduates seeking hands-on experience, emphasize willingness to learn, support pharmacy activities, and gain practical skills.
Clinical Pharmacist Objective : Aimed at pharmacists specializing in clinical roles, emphasize expertise in medication therapy management, patient counseling, and interdisciplinary collaboration.

Conclusion:

A well-crafted pharmacist resume objective is a powerful tool for capturing the attention of potential employers. By tailoring the objective to the specific job and showcasing relevant skills and experiences, candidates can effectively demonstrate their value and stand out in a competitive job market.

Whether you’re a fresh graduate, an experienced pharmacist, or a professional seeking a career change, the right resume objective can make a significant impact on your job search success.

Remember, your resume objective is your first opportunity to make a strong impression. It’s a chance to convey your passion for pharmaceutical care, highlight your unique strengths, and align yourself with the needs of the hiring organization.

So, take the time to revise your resume objective using the tips and examples provided in this blog post. By doing so, you’ll increase your chances of landing your dream job and embarking on a fulfilling career in the pharmaceutical industry.

55+ Career Objective for Video Editor To Land Your...

91+ Best Electrician Resume Objective To Illuminate...

How to write an Appealing Career Objective For Resume?

85+ Career Objective For CSE Freshers To Propel Your...

69+ Objective For Customer Service To Unleash Your...

100+ Creative Carpenter Resume Objective To Elevate...

About the author.

Jessica William

Resume Examples

Common Tasks & Responsibilities
Top Hard & Soft Skills
Action Verbs & Keywords
Resume FAQs
Similar Resumes

Common Responsibilities Listed on Pharmaceutical Resumes:

Research and Development: Conduct research to develop new drugs and improve existing ones. This involves laboratory experiments, clinical trials, and data analysis to ensure the safety and efficacy of the drugs.
Quality Control: Ensure the quality of drugs produced by the company. This involves testing samples of drugs for purity, potency, stability, and safety. Any deviations from the set standards must be identified and corrected.
Regulatory Compliance: Ensure that all activities of the pharmaceutical company comply with local and international laws and regulations. This includes keeping up-to-date with changes in regulations and implementing necessary changes in the company's operations.
Production Planning: Plan and oversee the production of drugs. This involves coordinating with other departments to ensure that the necessary raw materials are available, the production process is efficient, and the finished products meet quality standards.
Product Launch: Plan and execute the launch of new drugs. This involves coordinating with marketing, sales, and other departments to ensure a successful launch.
Post-Market Surveillance: Monitor the safety and effectiveness of drugs after they have been launched. This involves collecting and analyzing data from patients, healthcare providers, and other sources.
Pharmacovigilance: Monitor and report any adverse effects of drugs. This involves collecting data from various sources, analyzing it, and reporting it to regulatory authorities.
Training and Development: Train and develop staff in the pharmaceutical company. This involves identifying training needs, developing training programs, and evaluating their effectiveness.

Speed up your resume creation process with the AI-Powered Resume Builder . Generate tailored achievements in seconds for every role you apply to.

Pharmaceutical Resume Example:

Led a team of researchers and scientists in the successful development and launch of a new drug, resulting in FDA approval and a 30% increase in market share within the first year.
Implemented a quality control system that reduced product defects by 20% and improved overall product quality, leading to increased customer satisfaction and repeat business.
Developed and implemented a training program for new employees, resulting in a 50% reduction in onboarding time and improved productivity.
Oversaw the production planning process, optimizing resource allocation and reducing production costs by 15% while maintaining high product quality standards.
Led the successful launch of a new drug, coordinating with marketing and sales teams to achieve a 25% increase in sales within the first quarter.
Implemented a post-market surveillance system, resulting in early detection and mitigation of potential safety issues, ensuring compliance with regulatory requirements.
Conducted extensive research and development activities, resulting in the discovery of a new drug candidate with potential for significant therapeutic impact.
Implemented a pharmacovigilance program, leading to the identification and reporting of adverse drug reactions, ensuring patient safety and compliance with regulatory guidelines.
Developed and delivered training programs for staff, resulting in improved knowledge and skills, and increased efficiency in day-to-day operations.
Drug development and launch
Team leadership and management
Quality control implementation
Employee training and development
Production planning and optimization
Resource allocation
Cost reduction strategies
Cross-functional collaboration with marketing and sales teams
Post-market surveillance and safety compliance
Extensive research and development
Pharmacovigilance program implementation
Adverse drug reaction identification and reporting
Regulatory compliance and guidelines
Staff training and development
Efficiency improvement strategies
Knowledge of FDA approval process
Risk management and mitigation
Strategic planning and execution
Project management
Data analysis and interpretation
Excellent communication skills
Problem-solving abilities
Attention to detail
Time management skills
Understanding of pharmaceutical market trends.

Top Skills & Keywords for Pharmaceutical Resumes:

Hard skills.

Drug Development Process
Good Manufacturing Practices (GMP)
Regulatory Compliance
Quality Assurance and Control
Clinical Trials Management
Pharmacovigilance and Drug Safety
Pharmaceutical Formulation
Pharmaceutical Analysis
Pharmaceutical Packaging
Pharmaceutical Manufacturing
Pharmaceutical Sales and Marketing
Pharmaceutical Research and Development

Soft Skills

Attention to Detail
Analytical Thinking
Problem Solving
Communication Skills
Time Management
Adaptability
Customer Service
Organization
Critical Thinking
Interpersonal Skills

Resume Action Verbs for Pharmaceuticals:

Implemented
Collaborated
Coordinated
Investigated
Streamlined

Generate Your Resume Summary

Resume FAQs for Pharmaceuticals:

How long should i make my pharmaceutical resume, what is the best way to format a pharmaceutical resume, which keywords are important to highlight in a pharmaceutical resume, how should i write my resume if i have no experience as a pharmaceutical, compare your pharmaceutical resume to a job description:.

Identify opportunities to further tailor your resume to the Pharmaceutical job
Improve your keyword usage to align your experience and skills with the position
Uncover and address potential gaps in your resume that may be important to the hiring manager

Complete the steps below to generate your free resume analysis.

Related Resumes for Pharmaceuticals:

Pharmaceutical manager, pharmaceutical rep, pharmacy tech, medical technologist, certified medical assistant, medical assistant, medical administrative assistant, medical support assistant.

Resume Builder
Resume Templates
Resume Formats
Resume Examples
Cover Letter Builder
Cover Letter Templates
Cover Letter Formats
Cover Letter Examples
Career Advice
Interview Questions
Resume Skills
Resume Objectives
Job Description
Job Responsibilities
FAQ’s

Pharmaceutical Resume Examples

If you are applying for a job in the pharmaceutical industry, having a well-crafted resume is essential for making a strong first impression with employers. Crafting a standout resume, however, can be a daunting task, especially when all the work experience is in a related field. Fortunately, there are countless examples of pharmaceutical resumes that can provide you with insight and guidance into what employers are looking for. With the right tips and tricks, you can create an impressive resume that will help you stand out and make a great impression. In this post, we’ll provide you with pharmaceutical resume examples and a writing guide to ensure you craft the perfect resume. You’ll learn how to capture the attention of employers, showcase your credentials, and make yourself stand out from the competition.

Resume Examples by Job-Title

Certified Pharmacy Technician
Clinical Pharmacist
Community Pharmacist
Intern Pharmacist
Lead Pharmacy Technician
Pharmacist Manager
Pharmacy Assistant
Pharmacy Buyer
Pharmacy Clerk
Pharmacy Intern
Pharmacy Manager
Pharmacy Technician Trainee
Registered Pharmacist
Retail Pharmacy Technician
Senior Pharmacy Technician
Staff Pharmacist
Analytical Scientist
Compounding Pharmacist
Hospital Pharmacy Technician
Long Term Care Pharmacist
Oncology Pharmacist
Compounding Pharmacy Technician
Inpatient Pharmacy Technician
Pharmaceutical Sales Representative
Pharmacy Cashier

Pharmaceutical Resume Headline Examples

A pharmaceutical resume headline is a concise summary of your professional experience, qualifications, and skills. It should highlight your abilities and provide a snapshot of your accomplishments in the industry. Crafting a strong headline can be the difference between getting noticed—or overlooked—by recruiters and hiring managers. When writing your headline, make sure that it accurately reflects your experience and qualifications in the pharmaceutical industry, such as certifications, relevant degrees, and job titles.

When writing your headline, use keywords from the job description. This will help the recruiter or hiring manager quickly identify your qualifications and background. Additionally, research the company’s website to find keywords that are relevant to your desired position. Use these keywords throughout your resume, including in the headline.

When writing your headline, include information about your job titles, professional accomplishments, and relevant experience. You may also include awards or certifications if they are relevant to the role. Include a few key words or phrases that demonstrate your expertise in the pharmaceutical industry.

Finally, use an active voice when writing your headline. This will help you stand out from other applicants and make your headline more memorable. Additionally, be sure to keep your headline succinct and to the point. Aim for one to two sentences that concisely summarize your experience and qualifications.

By following these tips, you can craft an effective pharmaceutical resume headline that will get you noticed by recruiters and hiring managers. Remember to include relevant job titles, experience, and qualifications in your headline. Additionally, use keywords from the job description and the company’s website to help you stand out from other applicants.

Pharmaceutical Resume Career Objective Examples

When crafting a resume for any position in the pharmaceutical field, it is important to include a career objective. A career objective is a brief statement that summarizes your qualifications, experience, and purpose for applying for the job. It should be written in a short, concise manner with well-crafted language that conveys a sense of your professional goals.

When writing a career objective for a pharmaceutical resume, the most important thing to keep in mind is that it should be tailored to the job you are applying for. This means that you should include information pertinent to your desired role in the pharmaceutical field, such as knowledge of medical terminology, familiarity with regulatory requirements, or experience in pharmaceutical manufacturing.

In addition to providing information about your qualifications and experience, a career objective should also convey your enthusiasm for the position. You should use language that is both clear and engaging to demonstrate your interest in the job and to make you stand out from other applicants. This can be achieved by using action verbs, such as “collaborating” or “coordinating”, to highlight your achievements and by expressing your desire to contribute to the success of the organization.

Finally, it is important to keep your career objective brief and to the point. A career objective should be no more than two sentences and should focus on the skills and experience that are most relevant to the job you are applying for. By following these guidelines, you can ensure that your career objective is effective in conveying your qualifications and enthusiasm for the position.

Pharmaceutical Resume Summary Statement Examples

The resume summary statement is your chance to make a great impression on potential employers. As a pharmaceutical professional, you should use this statement to highlight your unique qualifications and experience. When you craft a summary statement, you should be sure to include any relevant certifications, awards, or other professional achievements. Additionally, emphasize the skills that make you a valuable asset to the company, such as being able to effectively manage large teams or to stay up to date on the latest pharmaceutical regulations.

When writing a resume summary statement for a pharmaceutical position, you should focus on how you are uniquely qualified to handle the duties of a pharmacist. Make sure to mention any esteemed awards or publications that you have been associated with and any specialized training or certifications that you have earned. This section is also a great place to mention any research or teaching experience you have in the pharmaceutical field.

It is also important to show hiring managers how your qualifications benefit them. Describe the ways you can help the company by listing the business skills, such as problem-solving or customer service, that you have developed over the years. You should also list any achievements that set you apart from other applicants, such as being able to consistently exceed sales targets or leading a successful project.

By showcasing your qualifications and achievements in the resume summary statement, you will give yourself a competitive edge and demonstrate your value to potential employers.

How to write Experience Section in Pharmaceutical Resume

One of the most important components of any pharmaceutical resume is the Experience section. This section provides employers with an insight into the candidate’s background and the skills they have accumulated from past jobs. A well-written Experience section will help a candidate stand out from other applicants and demonstrate to employers that they are an ideal fit for the position.

When writing a pharmaceutical resume, it is important to include relevant experience that is related to the pharmaceutical industry. This experience should be listed chronologically, starting with the most recent. It is also important to provide sufficient detail on each job, including the duties and responsibilities held and the results achieved. When applicable, include any special projects, awards, certifications, or promotions that took place during the employment period.

Using specific keywords can also be beneficial when writing a pharmaceutical resume, as it helps employers quickly identify that the candidate has the necessary skills and expertise to fulfill the job requirements. Be sure to include industry-specific terms and terminology in the Experience section to demonstrate a thorough understanding of the role.

Finally, it is important to avoid listing anything irrelevant or unrelated to the position. Make sure to focus on the current job responsibilities, as this is the information that employers are looking for. By taking the time to craft a detailed and accurate Experience section, a candidate will have a greater chance of obtaining the job they are applying for.

Pharmaceutical Resume Writing Tips

When it comes to crafting a pharmaceutical resume, there are a few key elements to keep in mind. It is important to highlight your experience and credentials that demonstrate your qualifications for the job you are applying for. Pharmaceutical employers are often looking for candidates who have experience working in the industry, as well as a strong understanding of the regulations and procedures that go along with it.

When writing your resume, it is important to highlight your education, certification, and any professional experience you have accrued in the field. Be sure to include any relevant certifications or degrees that you have earned, such as a Bachelor’s in Pharmaceutical Science. This will demonstrate your commitment to the industry and your knowledge of the regulations and procedures that govern it. Additionally, any relevant work experience can be included, such as internships or jobs in the industry.

It is also important to include any relevant skills you have in the pharmaceutical industry. This can include any additional training you have received, such as specialized software or programs, as well as any expertise you have acquired in the industry. Additionally, be sure to include any certifications that you have achieved, such as a Pharmacy Technician Certification.

Finally, it is important to include any relevant professional memberships or affiliations you have in the industry. This will demonstrate your commitment to the field and your dedication to staying up-to-date with the latest developments in the industry. Additionally, any awards or recognitions you have earned for your work in the industry should also be included.

By following these tips, you can ensure that your pharmaceutical resume is both comprehensive and professional, and will help you stand out from the competition.

Pharmaceutical Career Prospects in the Industry

.The pharmaceutical industry offers a wide range of exciting career prospects for professionals. In a field that is constantly evolving and adapting to new technology, the need for well-trained and knowledgeable individuals is in high demand. With the right qualifications and experience, professionals can find themselves on the cutting edge of medical advances that lead to improved treatment options for patients.

Those interested in a career in the pharmaceutical industry should be aware that there is a wide range of roles available, from drug development and manufacturing to distribution and sales. Professionals should also be aware of the importance of regulatory compliance and the need for effective management of drug safety and efficacy. A comprehensive understanding of the industry and its regulations is essential for a successful career.

A well-written pharmaceutical resume is an invaluable asset in a competitive job market. It should include a detailed list of qualifications, experience, and relevant certifications, as well as a clear explanation of the candidate’s skills and competencies. It is important to include a list of accomplishments and awards, as well as any previous roles in the industry. Additionally, the resume should highlight any specializations or areas of expertise.

Understanding the industry and the role you’re looking for is essential for a successful career in the pharmaceutical industry. With the right qualifications and a well-crafted resume, the prospects for success in the pharmaceutical industry are excellent.

In conclusion, the pharmaceutical industry is an important and growing field, and having a well-crafted resume is essential to your success. This guide provides you with the information you need to create a standout resume that will help you stand out in the industry and land your dream job. With the tips and examples provided, you will be one step closer to achieving your career goals.

Resume Builder

Resume Experts
Search Jobs
Search for Talent
Employer Branding
Outplacement
Resume Samples

Pharmaceutical Resume Samples

The guide to resume tailoring.

Guide the recruiter to the conclusion that you are the best candidate for the pharmaceutical job. It’s actually very simple. Tailor your resume by picking relevant responsibilities from the examples below and then add your accomplishments. This way, you can position yourself in the best way to get hired.

Craft your perfect resume by picking job responsibilities written by professional recruiters

Pick from the thousands of curated job responsibilities used by the leading companies, tailor your resume & cover letter with wording that best fits for each job you apply.

Create a Resume in Minutes with Professional Resume Templates

Maintain, clean and organize work area and participate in safety improvement projects
Maintain, clean, and organize work area and participate in safety improvement projects. Properly dispose of waste product and containers
Work with the other pharmaceutical operators and supervisors in that area to establish priorities and meet deadlines
Perform work on personal computer (i.e., business operating systems, email, Microsoft software, etc.)
Work with the other pharmaceutical operators and supervisors in assigned area to establish priorities and meet deadlines
Maintain, clean, and organize work area and participate in safety improvement projects
Perform work, on personal computer (i.e., Business Operating Systems, read and respond to electronic mail in a timely manner, Microsoft Software, etc.)
Provides back up to Account Manager in areas of reporting, coaching, mentoring and sharing of best practices
Candidate sourcing, recruiting and screening
Interview and assess internal & external candidates (phone screens and in-person) using behavioral, competency-based interviewing techniques
‘Sell' candidates to hiring managers based on passive recruiting and/or phone interview results
Consistently consult and collaborate with hiring managers regarding expectations, challenges and strategies
Consistently consult with hiring managers regarding expectations, challenges and process improvements
Database Management; consistently reviewing pipeline for each requisition and dispositioning candidates accordingly
Achieve contract performance goals and objectives for geographical assignment as established in the client agreement
Deliver product messages to prescribers and office personnel within established policies, procedures, standards, and workflows
Engage physicians in telephonic interactions and deliver product messages to prescribers within established policies, procedures, standards, and workflows
Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in telephonic dialogue
Foster ongoing trust with HCP/Physician, consumer or pharmacy as relationship develops to facilitate the decision making process
Develop superior product and disease state knowledge to effectively educate and engage healthcare professionals in two-way dialogue
Develop a daily/weekly call schedule to insure efficient and comprehensive coverage of territory
Relevant professional qualifications are advantageous
Extensive EMP product knowledge
Demonstrates the highest levels of integrity and a strong work ethic at all times
Have good IT skills (MS Office, PowerPoint etc)
Perform basic math calculations
Ability to utilize hand tools to assemble and disassemble various types of machinery
Ability to follow instructions and procedures (SOPs, cGMPs)
Experience of operating in a highly automated environment and safe handling of
Proficient reading and comprehension skills
Decision-making, technical and problem solving skills

15 Pharmaceutical resume templates

Read our complete resume writing guides

How to tailor your resume, how to make a resume, how to mention achievements, work experience in resume, 50+ skills to put on a resume, how and why put hobbies, top 22 fonts for your resume, 50 best resume tips, 200+ action words to use, internship resume, killer resume summary, write a resume objective, what to put on a resume, how long should a resume be, the best resume format, how to list education, cv vs. resume: the difference, include contact information, resume format pdf vs word, how to write a student resume, director pharmaceutical quantitative research resume examples & samples.

Work with President to establish a profitable growth strategy and business development plan for the Quantitative research division
Develop and execute plans to achieve revenue and profit targets
'Own' the numbers understand and reinforce the link between operational procedures and financial results (i.e. billability, working capital goals, effective resource allocation)
Identify ways to improve and operationalize processes to optimize efficiencies and effectiveness
Personally manage and execute quantitative studies, with priority against complex, higher level strategic projects
Assume overall responsibility for the quality of the service and product provided by the quantitative team to inspire and stretch the thinking of the quantitative team regarding the translation of the client need into a compelling quantitative offering and insight deliverable
Make focused plans for Business Development activities that align with corporate strategy responsible for developing a strategy for the quant offering and leading an implementation plan across our target accounts (both existing and new) in order to achieve the targeted budget
Lead the proposal response thought process to RFPs on stand-alone Quantitative projects work alongside the proposal response team in shaping our quantitative design recommendations for integrated Qual/Quant projects
With prospective and existing clients, proactively identify service and/or product opportunities (beyond projects) that can entrench client relationships, i.e. infiltration strategies
Demonstrate leadership internally and externally by providing vision for the team and serves as a role model within the organization, embodying the values of collaboration/teamwork, superior customer service and excellence

Associate Director Pharmaceutical Market Research Resume Examples & Samples

Designs advanced quantitative research studies (tracking studies, single-purpose questionnaires, DCM, pricing studies, etc) with limited overview by senior staff, and with input as necessary from advanced methodologists consulting on the project
Writes screeners/questionnaires, including those for studies with advanced methodologies
Conducts data analysis via SPSS and provides direction on analysis/data manipulation to junior staff
Analyzes results and prepares visually compelling and clear summary reports with minimal guidance
Demonstrates understanding of advanced methodologies, and works on analyses (discriminant, cluster, conjoint, perceptual mapping)
Develops conclusions and marketing implications with minimal or no guidance from senior staff

Fraud Investigation & Dispute Services Manager Pharmaceutical Resume Examples & Samples

A bachelor's degree in economics, accounting, finance, law or other related field, and approximately 5 years of related work experience; or a graduate degree in economics, accounting, finance, or law and 4 years of related work experience
At least 1 professional designation (e.g., CPA, CFA, CFE), required
A minimum of 3+ years of relevant, forensic accounting, compliance, forensic technology or dispute related experience, preferably with a professional services firm, a boutique firm, or a consumer and industrial products organization
Experience managing staff on multiple projects and providing direction to team members; experience conducting project progress meetings with clients
Ability to develop detailed work plans, manage multiple projects, and lead team members
Strong financial, analytical, technical, and interpersonal skills
Excellent business development and client acquisition skills; strong presentation skills
Substantial knowledge of PC-based analytical tools, including databases (Access) and spreadsheets (Excel)
Knowledge of professional standards applicable to the profession and/or area of specialization

CIB Equity Research Pharmaceutical Research Associate Resume Examples & Samples

Support the senior Pharmaceutical analyst covering over 20 companies by conducting due diligence on the companies involved
Responsible for dealing with clients, sales, and trading, as well as preparing research reports for initiations of coverage, analysis of clinical trial data, earnings results, and industry news
Responsible for conducting physician conference calls and surveys to evaluate recent trends in medical practice
Building and maintaining financial models used to forecast sales of therapeutics drugs and earnings growth for the company
Attend industry conferences to analyze clinical trial data and assess the impact of changing regulation on the industry
Build company and market models to forecast prescription trends, project company revenues and account for ongoing consolidation in the industry
Occasionally prepare industry reports outlining up to date treatment practice for various medical diseases
Assist internal sales and trading teams in the timely analysis of breaking news in the sector
The candidate must have 2+ years of experience in Pharmaceuticals/Biotechnology and more specifically knowledge of the industry, as well as an understanding of the scientific mechanisms of action of drugs
Must have a demonstrated ability to analyze clinical trial data, as well as the ability to understand the scientific rationale as to why a certain drug represents promise as a new treatment for a certain medical disease
Must have the ability to conduct detailed physician interviews and surveys with regard to the mechanism of action of drugs, their promise as potential new treatment options, and where they might fit into medical practice in the future
Must have the ability to analyze and predict industry trends and determine their impact on stock prices
Must have experience using IMS/NDC prescription data to track the use of medical drugs
2+ years utilizing Excel for: Building/Maintaining Financial models - advanced level of excel proficiency is expected and required
2+ years experience in Company valuation preferably in a Research Capacity – buy/sell-side
2+ year demonstrated writing experience in a professional capacity – i.e.: Crafting Equity Research notes/correspondence; professional editor; journalism; blogging

Am-equity Pharmaceutical / Biotech Analyst Resume Examples & Samples

Research companies and industries. Cover the given universe of companies
Make relative valuation comparisons and investment recommendations to portfolio managers
Participate in managing regional and global analyst funds
Work and communicate with a global network of JPMIM analysts
Strong understanding of financial markets and securities valuations
Buy-side experience preferred
Ability to deliver clear/concise investment recommendations under significant uncertainty
Ability to distinguish between essential and nonessential information
Strong spreadsheet modeling skills
Excellent oral and written skills. Ability to work effectively with colleagues based in New York, London and Tokyo
At least seven years of relevant experience analyzing companies in the Healthcare industry
Educational background: CFA

Pharmaceutical Technician Resume Examples & Samples

Deal with customer queries and process order requirements
Maintain good customer relationships
Procurement activities working with Global Sourcing Network
Ensure the EMP Service customer's orders are managed in a correct manner and ensure all relevant regulatory paperwork is supplied to the company before a customer order is processed
Take & reply to customer queries in a timely manner. Immediately inform EMP Service Manager if you cannot resolve customer requests and ensure all requests are followed through
Maintain and have available at all times a daily EMP Service Diary/Log
Maintain the EMP Service Product File with all relevant bodies
Obtain and maintain the EMP Service Database of SPC's, PIL's and COA's
Control and process suppliers paper work and collate all relevant data
Ensure that all necessary manufacturing information is recorded in accordance with IMB Regulatory Reporting
Document and Report ADR's (Adverse Drug Reactions) to the EMP Service's Manager and the company's Responsible Person
Document and Report Product Recalls to the EMP Service's Manager and the company's Responsible Person
Comply with all GDP processes and procedures and in particular comply with regulations in force relating to supply of EMPs
Ensure that the EMP Service complies at all times to SOP's and Policies
Assisting in the coordination, implementation and follow up of regulatory agencies, internal audits and customer audits
Provide procurement support for other procured goods as required
To assist with all aspects of administration associated with the commercial team to include sales reports when required
Any other related activities as indicated by the EMP Service Manager
Required: Deep understanding of all issues specific to the supply of EMPs and must have
Previous experience with SAP is a distinct advantage
Flexibility: It is essential that the candidate be able to provide flexibility to the function. Specifically, this may require extra hours during busy periods
Must have 3 years minimum experience is a customer service role in the pharmaceutical sector
Requires clear diction and a good telephone manner and a commitment to excellent customer service

Principal Pharmaceutical Scientist Resume Examples & Samples

Manages and oversees the development of drug substances and drug formulations and/or transfer of development activities (including sterile products) with Shire contractors
Selects external Shire contractors as well as manages the day-to-day contractor activities
Monitors/supervises the manufacturing of drug products and drug substances (including sterile products) with Shire contractors
Writes/reviews protocols for manufacturing drug substances and drug products ( including sterile products)
Writes CMC documents for registration purposes, including CTAs, IMPD, MAA, NDA and responds to agency questions
Provides any necessary support to line manager as required
Provides technical input for selecting external Shire contractors as well as managing the day-to-day contractor activities
Assists in the review and evaluation of CMC documents during a due diligence exercise
Uses DOE and QbD principles in developing robust API and Finished Product manufacturing processes
Bachelor’s degree from college or university in Chemistry, Chemical Engineering, Pharmacy or closely related field and at least 7+ years experience in the Pharmaceutical Industry
M.S. in Chemistry, Chemical Engineering, Pharmacy or closely related field and 5+ years experience in the Pharmaceutical Industry
PhD in Pharmaceutical Sciences, Chemical Engineering, Pharmaceutics or closely related field and 3+ years of pharmaceutical industry experience
Proven working knowledge of current GMP regulations
Basic knowledge of European and/or US regulatory requirements for drug products
Knowledge of current pharmaceutics technology, including formulation and manufacture of solid, liquid and semi-solid dosage forms. Sterile product experience is highly desirable
Experience in robust process development, scale-up, manufacturing and validation, including DOE and QbD
Working knowledge of API synthesis and manufacturing is desirable and ability to liase with synthethic chemistry experts and coordinate API and finished product activities
Knowledge of clinical supplies requirements and regulations
Must have a working knowledge of various analytical methods used during the development of pharmaceutical products, including, but not limited to, HPLC, IR, UV, NMR, Mass Spec., dissolution and tablet hardness, etc., and ability to liase and coordinate development activities with analytical chemistry experts
Experience of early and late stage product development including product stability, product packaging and labeling requirements. Sterile product experience is highly desirable
Must be able to apply product development expertise to CMC sections of the regulatory filings
Project Management experience in a product development environment
Requires strong attention to detail in composing and proofing materials, establishing priorities, scheduling and meeting deadlines
Ability to present complex issues well in oral and written form
Ability to work independently, take initiative and complete tasks to deadlines
Excellent interpersonal, communication, analytical, and organizational skills
Ability to effectively present information to management, external contractors and employees at all levels of the organisation
Developing leadership skills
Basic knowledge of project leadership tools including MS Project

Associate Director, Pharmaceutical Analysis Resume Examples & Samples

60% Analytical Subject Matter Expert
In support of product development, apply broad and deep analytical knowledge and experience to the material characterization and testing of APIs and drug products
Apply knowledge and direct experience with the analytical support of synthetic peptides, oligonucleotides, and sterile products to ensure the appropriate analytical methodologies are in place and fit-for-purpose to properly support the development projects
Provide technical guidance for troubleshooting / investigating complex issues regarding analytical, stability, and process / product development
Leverage fundamental understanding of formulations, product development, and material characterization to implement analytical methodologies as appropriate for various formulations and dosage forms
Apply statistical analysis for interpretation of analytical and stability data
Author and/or review analytical methods and associated development, qualification, validation and transfer protocols and reports
Author and/or review release, in-process and stability specifications for APIs and drug products
Manage and oversee stability and analytical studies for projects. This includes authoring / reviewing protocols and reports as well as evaluating the results and leading technical discussions with project team members and external contractors
Ensure all cGMP data generated for development projects are managed and evaluated as described in relevant internal procedures and regulatory requirements
Quickly and effectively resolve complex analytical issues and deviations / investigations
Effectively communicate complex technical issues and deliver concise presentations to management and non-technical stakeholders
Actively contribute to the preparation and coordination of internal audits and regulatory inspections
Provide technical input for selecting external Shire contractors and manage day-to-day contractor activities for respective projects
Create and enhance collaborative and trusting relationships internally and with personnel at Contract Research Organizations (CROs)
Serve as a peer-leader to motivate / inspire colleagues and to mentor others in various aspects of analytical and problem-solving methodologies
Maintain a high level of professional and technical expertise through familiarity with scientific literature, conference attendance, and participation in training courses
20% Regulatory Submissions
Author and/or review relevant API and drug product CMC sections for global regulatory submissions (IND/CTA and NDA/MAA and annual reports) and ensure sections meet submission ready standards regarding content and format
Assist with responses to regulatory agencies regarding stability and analytical-related inquiries
Maintain awareness of current trends regarding global regulatory CMC requirements through literature and conference attendance
20% Documentation / Compliance
Ensure analytical test methods, development reports, and specifications are compliant with internal procedures and regulatory requirements
Assist in the development and implementation of departmental processes, procedures and policies
Maintain adherence to departmental and quality systems, such as SOP training records, deviations/investigations, CAPAs, and Change Controls
Supervise / coach less experienced staff as needed
Requires an advanced degree (MS or PhD) in Chemistry, Chemical Engineering, Pharmacy or closely related field and at least 8 years of relevant analytical experience within the Pharmaceutical Industry
The following items are essential
Direct experience with the analytical support of synthetic peptides or oligonucleotides
Experience with analytical support of sterile products
Strong knowledge of ICH and other regulatory guidelines
Knowledge and experience with product development and clinical supplies processes
Knowledge and experience with statistical applications for data evaluation
Experience in authoring analytical-related CMC sections of IND/IMPD and NDA/MAA regulatory submissions
Experience working with Contract Research Laboratories
Proven experience with various quality systems (e.g. investigations / deviations, CAPAs, change controls, etc.)
The following items are preferred
Knowledgeable in European and US CMC regulatory requirements for APIs and drug products
Familiarity with MHRA / FDA inspections and compliance experience

Pharmaceutical Category Consultant Resume Examples & Samples

Work collaboratively with other team members to ensure the completion of competitive and strategic sourcing projects for generic pharmaceuticals, Over-The-Counter (OTC) products and other related goods
Monitor and report on Humana’s pharmaceutical purchases, pricing, cost of goods sold and margin metrics
Manage the day-to-day activities associated with Humana’s generic pharmaceutical and OTC product supplier relationships, as assigned
Ensure Humana’s pharmacy distribution locations have access to quality pharmaceuticals and OTC products from reputable sources of supply
Identify and analyze product access and cost of goods improvement opportunities associated generic pharmaceutical & OTC product manufacturers, distributors and group purchasing organizations
Perform competitive pricing analyses to ensure Humana’s generic pharmaceutical & OTC product pricing is competitive across different sources of supply
Utilize internal and external industry data for category management reporting and analysis to help make appropriate business decisions
Track and reconcile financial metrics within supplier agreements
Manage supplier agreement business terms and conditions to ensure that both Humana and supplier are adhering to the terms of the contractual relationship
Assist with developing and documenting PSC processes as well as ensuring all PSC, HPS, and Humana processes are followed in the completion of work
Develop communication processes and tools to communicate with multiple pharmacy operations and inventory teams on product awards, contract adherence, etc
Develop and implement processes, methodologies and tools to forecast and model financial opportunities and communicate with business partners
Bachelors Degree in Finance or Related Field
2-3 Years of Pharmaceutical Procurement, Pharmaceutical Contracting or Pharmaceutical Supply Chain Work Experience
Proficiency in Financial Modeling
Intermediate or Advanced Proficiency in MS Excel
Knowledge of MS Office, Access and other data analysis tools
Previous Generic Pharmaceutical and OTC Procurement & Contracting Experience
Masters or MBA Degree Preferred
Six Sigma and CPM Certification Preferred

Tax Senior Pharmaceutical Company Resume Examples & Samples

Income Tax Compliance - Preparation of Corporate and Partnership return workpapers (federal and state) including calculation of estimated payments
Income Tax Provision – Help with the calculation of book tax differences for the YE provision
Indirect Taxes – Aid in the uploading of data for external preparation of sales & use tax returns as well as GST/HST/QST and gross receipts tax
Tax Controversy – Assist with gathering data for ongoing tax audits
Tax Research – review tax issues and aid Tax Manager with research projects
2-5 years of public accounting or relevant pharmaceutical industry experience
Big 4 preferred
SAP preferred
Excellent presentation, verbal and written skills a must
CPA or parts passed a plus

Head of Quality, Pharmaceutical Resume Examples & Samples

A minimum of a Science, Pharmacy, or equivalent honours degree and will be eligible to be licenced as QP under European Directives
At least 5 years of experience in a quality or production function within the pharmaceutical industry
Previous supervisory/management and QP experience is advantageous
Good knowledge and experience of pharmaceutical manufacturing processes and quality systems is required, including qualification, validation, change control and regulatory affairs
The person should be a demonstrated self-starter and motivated, with a dynamic, hands-on approach and must be improvement focussed
Excellent communication, organisational, interpersonal and teamwork skills are necessary along with the capacity to manage deadlines and make key quality decisions

Pharmaceutical Clean Utilities Technician Resume Examples & Samples

Bachelor’s degree in Engineering
5+ years of postgraduate experience in the maintenance and operation of a pharmaceutical or biotechnology company
Flexibility to work night shifts as required

Senior Principle Pharmaceutical Scientist Resume Examples & Samples

Manages and oversees the development of drug substances and drug formulations and/or transfer of development activities with Shire contractors
Helps develop and manage budgets for R&D projects
Responsible for providing guidance to Shire contractors
Monitors/supervises the manufacturing of drug products and drug substances with Shire contractors
Writes/reviews protocols for manufacturing drug substances and drug products
Writes/reviews analytical method protocols and stability protocols
Writes CMC documents for registration purposes, including CTAs, IMPD, MAA, and responds to agency questions
Is an active member of Project Teams and supports the Supply Chain PSL locally on marketed products
Assists in the development and implementation of departmental processes, procedures and policies
Bachelor’s degree from college or university in Chemistry, Chemical Engineering, Pharmacy or closely related field and at least 7+ years experience in the Pharmaceutical Industry, or a M.S. in Chemistry, Chemical Engineering, Pharmacy or closely related field and 5+ years experience in the Pharmaceutical Industry, or a PhD in Pharmaceutical Sciences, Chemical Engineering, Pharmaceutics or closely related field and 3+ years of pharmaceutical industry experience
Must have 3+ years experience in pharmaceutical formulation development and/or manufacturing for late stage clinical development candidates in oral solid dosage forms

Accounting Manager With a Pharmaceutical Company Resume Examples & Samples

Responsible for month end close, prepare journal entries and present work to senior management as it relates to the Revenue and related expense
Assist in budgeting and related projects
Prepare audit schedules and interact with auditors
Supervise Staff Accountants
Responsible for financial statement reporting to Corporate
Manage Reporting and industry profitability
5-7 years of general accounting and related experience in a pharmaceutical company and/or public accounting
Revenue and expense accounting experience a plus; Gross to Net Reporting a plus
Large Corporate experience
BA in Accounting, CPA a plus
SAP experience a plus
Proficiency with GL software, Excel and Word

Pharmaceutical Industry Specialist Banker Resume Examples & Samples

Acted as a coverage banker for Pharmaceutical Industry
Promote M&A business
Promote License business
Strong knowledge of Pharmaceutical Industry
Coverage Banking, M&A or ECM experience
Native level fluency in written and spoken Japanese based in Japan with Business English
Masters Degree ( Phd . better ) in Life Science related field
Working experience in Pharmaceutical Industry
Global Investment Bank experience

Senior Pharmaceutical Editor Resume Examples & Samples

5+ years of Writing and Editing experience
Bachelor's Degree in English or Communications
Comfortable marking up edits digitally via Adobe PDF
Agency or CME (continuing medical education) experience
Previous experience within the Pharmaceutical industry

Inside Pharmaceutical Sales Representatives Resume Examples & Samples

Engage physicians and office personnel in live video detail and/or telephonic interactions
Able to influence prescribers in an effort to significantly grow market share
Adhere to regulated guidelines for communications via all channels
Maintain a high level of product knowledge, policies, procedures, contacts, and the medical device industry; continual learning & training as required
Ability to build strong relationships with key staff members and establish relationships with the appropriate personnel in the physician’s office
Ensure timely and appropriate communication occurs with client’s sales and marketing team
Display flexibility and willingness to accept constantly changing project/program updates
Demonstrate corporate values on a consistent basis
Extensive self-study, training and testing are required; eligibility to proceed through training and selling certifications are dependent upon passing required exams
Adhere to all company policies and guidelines
Superior rapport and relationship building skills with the gatekeeper and office personnel
Demonstrated ability to learn, retain, and articulate technical/scientific-product related information and provide unscripted responses on appropriate subject matter
Powerful customer-first focus
Planning efforts are well thought out and result in directly influencing a strategic selling approach

Pharmaceutical Development Lead Resume Examples & Samples

Responsible for selecting external Shire contractors as well as leading the team managing the day-to-day contractor activities
Responsible for providing strategic guidance regarding drug substance and drug formulation development to Shire project teams
Leads the development of drug formulation with Shire contractors
Leads the manufacturing of drug substances and drug products with Shire contractors
Reviews protocols for manufacturing drug substances and drug products
Writes and/or reviews analytical method development and stability protocols and reviews resulting data
Ensures development of robust chemical and finished product processes through the use of operational excellence tools such as DOE and QbD
Responsible for managing and developing reporting staff
Participates and contributes to Due Diligence assessment of potential product licensing or company acquisition opportunities as required
Delivers CMC Quality Documents (Module 3 and relevant part of Module 2) and supports the QA department by providing regulatory annual updates, ensuring full compliance with relevant regulatory authority quality standards
Leads or contributes to R&D Process improvement initiatives
Participates in Shire Product Strategy and Project Teams. In some circumstances, may be requested to act as the PST-L (Product Strategy Team Lead) for R&D functions
May be a key member of joint Development Committees with partner development organizations
Leads and assists in the development and implementation of departmental processes, procedures and policies
Is an active member of the Pharmaceutical Sciences Leadership Team
May deputize for the VP, Product Development in various R&D staff meetings and tasks
Bachelor’s degree from an accredited college or university in Chemistry, Chemical Engineering, Pharmacy, or closely related field
Generally has at least 12 years’ experience (or 10 years plus PhD) in the Pharmaceutical Industry
Must have a least 10 years’ experience in formulation development and/or manufacturing

Pharmaceutical Patent Litigation Attorney Resume Examples & Samples

Experience in ANDA litigation
Must be able to perform legal research and write persuasively
Deposition and trial experience is a plus

Pharmaceutical Copywriter Resume Examples & Samples

2-3 years of advertising agency experience
Ability to perform basic tasks in Adobe Creative Suite
DTC experience
Natural storytelling skills
Excellent presentation / public speaking skills
Digital (website) and print (long forms) experience
A creative portfolio of work showing own brand concepts and campaigns
Prior experience in healthcare

Senior Pharmaceutical Copywriter Resume Examples & Samples

5+ years of relevant professional experience
TV production experience, including directing voice-over talent
An impressive portfolio of work showing at least six examples of own brand concepts and campaigns
Experience developing big digital and social conceptual ideas
Creative and collaborative mindset

Account Supervisor Pharmaceutical Advertising Resume Examples & Samples

Lead day-to-day management of projects, as well as overall account management, including
Run internal and external meetings, ensuring agreements are met
Ensure projects meet client, agency and regulatory requirements
Manage budgets and timelines effectively
Forge strong client relationships with Creative, Production, Planning, other agency departments and partner companies
Evaluate the input and ideas of Creative, Planning and Media relative to strategy and client preference
Act as key category expert about client business and brand performance
Act as contact for client research plans and implementation
Compile billing and income forecasts and reports
Mentor and manage junior staff
5+ years pharmaceutical advertising experience, including both HCP and DTC—a solid knowledge of the business is required
Strong ability to lead, applying clients’ strategic priorities and business objectives to daily activities and tactics by way of exceptionally effective communication
BA or equivalent degree is required

Project Manager Pharmaceutical Advertising Resume Examples & Samples

Coordinate and manage multiple projects from conception through completion
Communicate scheduled deadlines and provide effective warning when delivery dates may be in jeopardy
Coordinate team briefings, internal reviews of creative, and all other meetings needed to complete any given project
Reinforce Agency process with all teams
3+ years agency project management/traffic experience; some pharmaceutical advertising experience required for this position
True problem solver—able to anticipate roadblocks and offer solutions
Highly detail-oriented while managing multiple tasks and tight deadlines with confidence
Exceptional interpersonal skills necessary to interact with a range of personalities and establish effective relationships at all levels of the organization

Project Management Supervisor Pharmaceutical Advertising Resume Examples & Samples

Help establish and maintain team operating principals, formalizing the team’s strategy, structure, processes, templates, and operating norms to implement department vision
Ensure proper scope allocation and adherence in conjunction with the Director of Operations, Senior Account Management, and Finance
Identify and suggest process improvements to enable efficiency
Interview prospective Project Management candidates
Train new and mentor existing Project Managers, providing guidance and coaching to assist in individual growth and development
Own a brand or brands as necessary based on scopes and staffing—either individually, or in a supervisory capacity with junior members of Project Management team
5+ years agency project management/traffic experience; 2+ years in a supervisory capacity—pharmaceutical advertising experience required
Keen understanding of advertising principles and creative project process terminology
Exceptional interpersonal skills necessary to interact with a range of personalities and establish effective relationships at all levels of the team and organization

Project Manager Pharmaceutical Resume Examples & Samples

Serve as liaison between Account Management, Creative, Studio, and other inter-agency partners
Communicate project requirements and procure supporting materials to ensure that projects move through the agency in a timely manner
Monitor and follow-up with all appropriate departments on project development
Initiate, develop, drive, and revise schedules
Familiarity with design applications

Pharmaceutical & Life Sciences Resume Examples & Samples

Delivering significant business results that utilizes strategic and creative thinking, problem solving, individual initiative and the following abilities
Leading project work streams, emphasizing the ability to build solid and collaborative relationships with team members and also work autonomously with little direction
Communicating effectively in written and verbal formats to various situations and audiences
Managing and conducting quantitative and qualitative benchmarking and primary and secondary analyses of large and complex data

Financial Accountant With Top Pharmaceutical Company Resume Examples & Samples

Acquisitions/Divestures
Distributions
University Degree in Business, Finance, or Accounting
Qualified Accountant
Minimum of three years of related accounting experience required
Language skills are preferable though not essential
Strong technical accounting skills i.e. good knowledge of accounting standards
Knowledge of US GAAP
Familiarity with Sarbanes Oxley and internal controls
3+ years of pharmaceutical ad agency experience
Bachelor's Degree in a related fields
Professional attitude
Experience writing for HCP and DTC
Experience writing for the insurance / healthcare industry

Director Custom Market Research Pharmaceutical Resume Examples & Samples

Bachelor Degree required. MBA/M.S./PhD preferred
3+ years performing Primary Market Research both qual and quant in healthcare / Pharmaceuticals
Significant experience with multivariate statistical analyses, SPSS and Excel preferred
Willingness and ability to travel out-of-state/out-of-country
Candidates must LOVE Market Research!

Accountant for MNC Pharmaceutical Company Resume Examples & Samples

Preparation of accurate monthly management accounts (including Income Statement, Balance Sheet, Cash flow statement and analysis)
Preparation of annual and quarterly financial accounts in accordance with US GAAP and with supporting schedules
Preparation of key management information to a high standard and perform financial analysis with meaningful insights as required
Support transition to company ERP system
Management Accounts
Key Management information
Financial Analysis
Statutory reporting
Maintaining general ledger
Bank reconciliations
Revenue recognition
Liaise with FP&A To provide business analysis insights
SOX compliance
Irish and US GAAP
Big four trained or top ten practice
Industry based clients

Director of Procurement for a Pharmaceutical Company Resume Examples & Samples

Partner with the CEO, Senior Management team on all operational and strategic procurement issues as they arise; provide strategic recommendations to the CEO based on metrics and projections, cost identification and allocation
Participate in the ongoing strategic planning process for the procurement and purchasing teams as an integral member of the senior management team
Oversee long-term budgetary planning and cost management in alignment with the strategic plan
Develop and manage strategic procurement plans present operational metrics both internally and externally as needed
Manage purchasing teams based on company goals and objectives
Increase income and decrease expenses through strategic planning, operational oversight and stringent financial analysis
Provide leadership and key negotiations with vendor contracts and mange vendor selection process based on company goals and company risk factors
Development and track departmental budgets and reforecasts

Hia-pharmaceutical Wholesaler Pricing Specialist Resume Examples & Samples

Evaluating enterprise DW architecture feasibility, risk and technologies related to business change (i.e. assessing, identifying and recommending BI and related business stakeholders' data requirements; BI solution prototyping and development; processes and performance from business and technical standpoints; and the impact of data changes on business and/or IT processes)
Advising CXO's on emerging BI/DW technologies and strategies consistent with clients' business strategies
Prioritizing, preparing and implementing BI and/or DW architectural improvements (i.e. developing and recommending alternative DW technical and data management solutions, methodologies, strategies and architectural improvement plans)
BI and enterprise DW data management, modeling, integration and/or synchronization, quality, security, conversion and analysis, star schema and relational reporting models, enterprise data management policies, procedures, compliance and risk management and/or database administration,
Design and development of data models, extraction code and cleansing routines utilizing typical data quality functions, i.e. standardization, transformation, rationalization, linking and matching that leverages data standards, processes and technology management for data, master data, and metadata; and, data security (including data masking and related data protection techniques)
Identification and addressing of client needs--developing and sustaining deep client relationships using networking, negotiation and persuasion skills to identify and sell potential new service opportunities; preparing and presenting complex written and verbal materials; and defining resource requirements, project workflow, budgets, billing and collection
Team leadership--generating a vision, establishing direction and motivating members, creating an atmosphere of trust, leveraging diverse views, coaching staff, and encouraging improvement and innovation

Pharmaceutical & Life Sciences Market Access Resume Examples & Samples

Global trends in market access and requirements for launch management
Key market requirements regarding access strategy, pricing and reimbursement, especially in the context of product launch or lifecycle management
Pricing and profitability strategy, price setting, and innovative contracting
Contracting and rebate modelling for the US market
Epidemiology and patient flow modeling
Target product profile development, unmet market needs, clinical end points to support pricing and market access strategy, country launch sequencing, and other pricing and market access factors
Short- and long-term forecasting
Budget impact modeling, including pharmacy and medical claims analyses
Portfolio optimization/rationalization
Pricing, contracting, and/or managed markets organizational and governance design; and,
Therapeutic areas across primary care, specialty, oncology, and generics
Developing pricing and profitability strategy emphasizing an extensive track record of managing large scale projects that involve thinking critically about the business model and processes, and articulating a vision for the future of the business through thought leadership
Identifying and addressing client needs; developing and sustaining deep client relationships using networking, negotiation and persuasion skills to identify and sell potential new service opportunities; preparing and presenting complex written and verbal materials; and defining resource requirements, project workflow, budgets, billing and collection
Leading and Overseeing complex projects related to pricing and profitability
Leveraging industry knowledge and analytical skills, especially as it relates to project management and project facilitation
Leading and/or facilitating teams and developing client proposals, leveraging extensive business development and relationship management knowledge
Interacting with senior leadership in client organizations
Leading teams to generate a vision, establishing direction and motivating members, creating an atmosphere of trust, leveraging diverse views, coaching staff, and encouraging improvement and innovation
Leveraging business transformation skills with a track record of successful change enablement with quantifiable results
Utilizing analytical skills with the ability to translate complex problems into simple and actionable tasks
Managing teams to identify and address client needs; communicating value propositions; managing resource requirements; preparing and coordinating complex written and verbal materials; managing project workflows and budgets; and,
Building and sustaining extensive client relationships using networking, negotiation and persuasion skills to identify and sell potential new opportunities, ideally in the $2-4 million range annually

Finance Assistant, Pharmaceutical Resume Examples & Samples

Processing of vendors' invoices, employees' expense claims, payment files; ability to follow up and resolve outstanding items and exceptions in a timely manner
Perform certain collection calls with customers to arrange payment of past due accounts
Processing cash application, customer master data maintenance, pricing adjustments, credit hold release, cash collection and other tasks
Responsible for the timely preparation of the month end closing procedures
Interacts successfully with internal and external auditors by providing timely & accurate data and communication
Helps develop, maintain and assess internal controls related to Gilead's accounting and financial reporting systems

Systems Support Engineer With a Leading Pharmaceutical MNC Resume Examples & Samples

Provide support for user requests and resolve various software and hardware issues
Configure, support, and maintain user desktops, laptops and printers
Perform basic server administration; security, file and directory permissions, adding/deleting users, etc
Work with senior staff to perform administrative and maintenance tasks for the corporations network/domain

Legal Counsel, Pharmaceutical Resume Examples & Samples

Working with the Business Development and sales team to negotiate new business contracts
Advising on a broad range of commercial contracts
Reviewing and revising existing contracts with vendors
Ensuring Compliance regulations are adhered to across the business
Managing external counsel relationships
5 years PQE
Experience in working in an international pharmaceutical company
Transactional Experience
Drafted and negotiated commercial contracts relevant to the Pharmaceutical Industry
Strong understanding of Compliance and relevant regulations

Pharmaceutical & Life Sciences, Commercial Resume Examples & Samples

Pricing techniques, strategies and processes
Pricing technologies and how they effect the overall pricing strategy
Writing, communicating, facilitating, and presenting cogently to and/or for all levels of industry audiences, clients and internal staff and management
Leveraging pricing knowledge and analytical skills, especially as it relates to project management, project facilitation, and the development of client proposals
Researching and analyzing pertinent client, industry, and technical matters, including leveraging the ability to problem-solve, prioritize, and manage multiple tasks simultaneously
Demonstrating self-motivation and responsibility for personal growth and development
Creating Excel models,
Drafting and presenting PowerPoint presentation decks

Janssen Pharmaceutical Ecldp Internship Summer Resume Examples & Samples

Complete project(s) with business objectives designed to accelerate and support market growth within marketing brand teams or key commercial functions
Demonstrate in depth understanding of critical issues, decision making, and project management skills
Collaborate with key internal and external stakeholders in support of project deliverables
Act with speed, learning agility, and accountability
Cultivate meaningful internal and external partnerships, adding value and insights for the organization
Take personal accountability for making Credo-based decisions and fostering a Credo-based culture
Present project results to senior leaders and management team at conclusion of internship
Candidate must be a graduate student completing MBA in 2018. Concentration in Healthcare Management is preferred
Minimum of 4 years of business experience in any industry is required
Experience in marketing, intelligence, sales, business analytics, strategic planning, and/or management consulting in health care related field is preferred
Experience working in a regulated environment is preferred
Excellent writing, presentation and communication skills is required
Proven analytical skills and cycles of success in a professional business environment is required
Ability to think strategically, influence, and be able to execute a plan effectively is required
Ability to work in a team environment with sound judgment, creativity and perseverance is required
Legally authorized to work in the United States without the need for sponsorship now or in the future is required.Administration

Scientist, Pharmaceutical Chemistry Resume Examples & Samples

Provide training in routine activities and methods
Take responsibility as required for elements of specific projects and/or specific areas of general laboratory/sample administration
Will be expected to work in different laboratories if the demand is required

Lead Bio-pharmaceutical Process Engineer Resume Examples & Samples

University degree
More than 10 years experience in executing bioprocess engineering for the pharmaceutical industry in leading functions
Experience in the execution of engineering for chemical synthesis and fill-finish projects according to GMP for parenteral production an asset
Significant years working in this sector, including experience in leading teams of junior and senior engineerss
Knowledge of microbiological and tissue cell elements is preferred
Ability to successfully interface directly with client personnel

Senior Bio-pharmaceutical Process Engineer Resume Examples & Samples

Fluency in the German and English language is a must, whilst French or any other language is an asset
University degree and engineering execution experience in process design of bio-pharmaceuticals
Significant years working in this sector, including some experience in leading teams of junior engineers
Knowledge of Microbiological elements is preferred
Knowledge and experience in Business Development would be highly beneficial

Pharmaceutical Coordinator Resume Examples & Samples

Assists in the preparation of routine protocols, informed consents, SOPs, and other appropriate documentation
Monitors clinical trials to ensure subject safety and compliance with the study protocol, FDA regulations and ICH/GCP Guidelines, may be done with supervisor
Coordinates necessary activities required to set-up, monitor, and close-out clinical trials sites
Conduct site assessment, initiation, routine, and close-out monitoring visits, may require supervision
Complete accurate monitoring visit reports
Develops training materials and conducts training for study implementation based on company policies and SOPs
Contributes to the development of and implements protocols and informed consents for research studies
Provides guidance on any protocol related issues
Manages and oversees budget for one or more research projects
Develops, reviews, and maintains key study documents to ensure adequate resource and reference documentation
May serve as a liaison with internal and external partners to ensure effective collaboration efforts
Oversees planning of meetings, site visits, and drafting necessary documents
Ensures compliance with government regulations when writing and reviewing protocols, analysis plans, reports, and manuscripts
Provides input with questionnaire development, analysis, study design, and material management
Bachelor’s degree or its international equivalent in Health, Behavioral, Life or Social Sciences or other fields related to international/ human development
Master’s degree or its international equivalent preferred
3 - 6 years of previous clinical research experience
Proficiency in Microsoft Office, spreadsheet software and other technology required
Articulate, professional and able to communicate in a clear, positive fashion with clients and staff
Must be able to read, write and speak fluent English
Must have a working knowledge of concepts, practices and procedures for conducting clinical research studies
Solid knowledge of software programs used to collect data and track risk based monitoring parameters
Ability to analyze and interpret data, identify errors and prepare reports
Exceptional attention to detail
Works on moderate to complex problems of diverse scope that require analysis or interpretation of identifiable factors
Demonstrates good judgment in selecting methods and techniques for obtaining solutions
Decisions may affect a work unit or area within a department
Provides suggestions on business and operational decisions that affect the department
May serve as team lead to team members
Typically reports to a Manager
Travel Requirements: Greater than 25% Typical Physical Demands
Effective clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Excellent understanding and demonstrated application of Good Clinical Practices and applicable Standard Operating Procedures
Effective organizational and time management skills
Effective interpersonal skills Proven flexibility and adaptability
Ability to work in a team or independently as required

Senior Counsel, Pharmaceutical / Healthcare Resume Examples & Samples

Comprehensive commercial contract drafting and negotiation skills, with Article II of the UCC knowledge preferred
Experience advising on healthcare transactions to ensure compliance with Anti-Kickback Laws
In-depth legal knowledge that allows for expeditious problem identification and resolution
Notable business acumen dealing with risk management and organizational savvy
Excellent interpersonal skills with an ability to provide sound, clear legal advice to clients
Aptitude to work well with larger team in seeking efficiencies for legal support
Ability to manage simultaneous projects in an efficient and timely manner
Outstanding verbal and written communication skills and attention to detail
10 years of experience
Experience with healthcare regulations will be strongly preferred
Blend of law firm and in-house experience will be preferred

Pharmaceutical Buyer Resume Examples & Samples

Work with the pharmacy to establish product/service requirements
Order pharmaceuticals and supplies for the pharmacy
Maintain all backorder information
Research and maintain statistics of all items missing from the pharmacy floor
Maintain and verify drug inventory controls are at a level to meet customer demand
Participate in drug inventories
Assist the call center management with customer issues and communications when drugs are out of stock
Verify and resolve outstanding purchase orders
BA/BS degree or six to eight years of relevant working experience
Up to two years of relevant work experience
Strong organizational skills and complex problem solving skills
Excellent verbal and written communication skills
Be able to work a flexible schedule to meet demand

Manager, Pharmaceutical Affairs Resume Examples & Samples

Supervision and training of the project managers involved in drug distribution. Identify provision of study agent for each protocol. For agents supplied by industry, forecast and monitor supply requirements, develop distribution plan (obtain and review proposals, review budgets, and integrate into overall budgetary plan), review labels and labeling requirements, develop plan for meeting shipping requirements (regulatory documentation) and develop protocol ordering instructions and forms. Responsible for development and maintenance of relevant SOPs
Pharmacovigilance: develop and maintain relevant standard operating procedures (SOPs), review expedited adverse event/IND safety reports, provide sponsor assessment of attribution for Alliance-held INDs to determine if expedited reporting to FDA is required, and submit expedited adverse event/IND safety reports to industry sponsors as required
Supervision of IND/IDE management: determining the need for an IND/IDE for a given trial, preparing initial IND submission, and supervising annual IND/IDE reporting. Develop and maintain SOPs for IND management. Recommend responses to FDA protocol review comments, compile responses to FDA, and facilitate FDA-required changes to protocols. Represent the Alliance in discussions and meetings with the FDA
Protocol Development: Review and draft as needed, sections on drug ordering, and expedited adverse event reporting requirements
Respond to questions from industry and Institutional Review Boards (IRBs) regarding drug supply, drug transfers, and assist with questions about informed consent modifications related to risk
Review agreements between the Alliance and research partners for compatibility/consistency with protocols, Alliance policies and procedures and feasibility of deliverables
Serve as a liaison to the Pharmacy Committee and Alliance disease and modality committees to assist in the development of clinical trials, as appropriate

Risk & Compliance Manager, Pharmaceutical Resume Examples & Samples

Directly report to the Finance Director
Involve in risk management planning activities and ensure that all activities are operating effectively and efficiently
Ensure internal policies are adhered to Glocal standard
Conduct anto-bribery, anti-trust and whistle blowing project to ensure compliance with finance and operation manuals
Handle ad-hoc projects
Occasional travel is required
Demonstrate comprehensive knowledge of all promoted products
Develop comprehensive and accurate sales presentations using all marketing and selling materials
Contact and deliver proficient sales presentations to a defined list of current and prospective customers
Pre and post call analysis of calls
Help to maintain required project documentation
Provide customers with product and service information
Minimum of 6 months sales experience - inside or business to business
Must possess excellent presentation and selling skills
Ability to prioritize and reprioritize workload depending program needs
Ability to multi-task between numerous websites and applications
Computer savvy - Windows environment, Word and Excel knowledge
Must type 35 wpm or better
Ability to work a shift between the hours of 8am and 8pm, Monday to Friday (40 hour work week)
Exposure to the pharmaceutical industry
Call Center Experience

Pharmaceutical Congress Meeting Manager Resume Examples & Samples

*This position can be virtual but the person hired must work west coast hours. ***
*You must have pharmaceutical congress experience to be considered for this position**
40% PROCESS MANAGEMENT: Reviews all supplier contracts prior to finalization, ensuring both program specific and generic terms and conditions are accurate, including attrition, cancellation policies, etc. Uses appropriate authorization and addendum form to ensure consistency and accuracy. Establishes a project timeline with a work flow schedule. Manages and negotiates hotel, housing bureau, air and all third party contracts. Monitors attrition dates, cancellation policies and ensures contracted services are executed. Communicates between Information Technology support and clients with respect to web requirements on assigned programs. Coordinates with creative team to produce program materials. Responsible for ongoing SOP documentation and updates
Partners with designated team to communicate registration and air needs and directions, status meetings and continuous communication throughout convention planning and execution. Coordinates all program details and production of a event itinerary/agenda. Works with accounting to complete final bill reviews prior to final invoice processing. Ensures consistency of client branding guidelines. Maintains accurate records, system input, and complete file management. Evaluates participation impact and reassesses objectives and outcomes; plans for continuous improvement. Outlines strategy, communication plan, and process for assigned conventions/congresses. Involved in management of all program phases including sourcing, contract negotiation, planning, and final bill completion, while maintaining high level of data integrity and timeliness
20% STRATEGIC LEADERSHIP AND RELATIONSHIP MANAGEMENT: Be a trusted advisor to client stakeholders across multiple business units; Develops overall congress plans/strategy and budgets for congress stakeholders; Creates best practices based on industry benchmarking and knowledge; Develops and reports on program metrics; Analyzes operational data to identify cost savings, operational efficiencies and advises on ways to maximize ROI
OTHER: May require travel to destinations worldwide, in support of client site inspections and/or program operations. There is an inherent risk associated with all travel, often as a result of extraordinary circumstances. Therefore, during an emergency, it is your duty to provide the necessary guidance and leadership, and to promote the safety of the client, travel participants and other Maritz employees by implementing or supporting prescribed crisis procedures. Keep abreast of industry standards and trends related to responsibilities
Minimum of 5+ years experience in event or meeting management required. Prior pharmaceutical congress planning experience required
Proven aptitude for technology and/or software solutions and data analytical skills
Ability to travel up to 20% of the time required
Proven ability to develop, manage, and maintain key client and supplier relationships
College degree or comparable experience required

Business Consulting Manager / Pharmaceutical Resume Examples & Samples

Partner with our leaders to drive business development and client relationships
Consistently deliver quality client services and drive high-quality work products within expected timeframes and on budget
Monitor progress, manage risk and ensure key stakeholders are kept informed about progress and expected outcomes
Effectively lead and motivate teams with diverse skills and backgrounds
Play an active role in counseling and mentoring junior team members within ZS
Demonstrate deep life sciences industry sector knowledge
Demonstrate deep functional expertise in marketing strategy
Demonstrate ability to quickly assimilate new knowledge
Possess in depth business acumen
Stay abreast of current business and industry trends relevant to the client's business
Remain current on new developments in advisory services capabilities and industry knowledge
Direct multiple projects simultaneously, honing analytic and project management skills
Motivate, coach and serve as a role model for project team members
Provide thought leadership and innovation within projects and across practice areas
Play a key role in development of consulting capabilities and offerings
MBA from a top university strongly preferred, with a record of strong academic performance
Approximately 4-6 years of prior management consulting experience, preferably in the healthcare/pharmaceutical industry
Demonstrated experience driving revenue within existing clients
Deep knowledge of strategic brand segmentation, targeting and positioning
Characteristics of a forward thinker and self-starter that thrives on new challenges and adapts quickly to learning new knowledge
Ability to lead a virtual team of consulting professionals across multiple projects; experience working with teams in India a plus
Ability to communicate clearly and effectively in oral and written form
Strong decision-making skills and the ability to influence others
Analytic problem solving skills, with an ability both to see the big picture and delve into details
Excellent organization & planning skills and willingness to travel to meet client needs

Scientist Within Bioprocess Pharmaceutical Development Resume Examples & Samples

You lead and coordinate pharmaceutical development activities (formulation, pharmaceutical processes incl. transfers and in-use studies) for parenteral dosage forms of NBEs and Biosimilars
Within the respective CMC Team you represent DP development and lead intermittent or support the multidisciplinary DP sub-team
According to project objectives, timelines and cost you ensure delivery of DP work packages and project support
Moreover, you ensure delivery of high quality data, presentations and reports including required documentation for regulatory filings (IND/BLAs)
Excellent communication to stakeholders (e.g. project team and line management) and excellent interaction and collaboration with interfaces (e.g. manufacturing sites) is ensured by you
You identify, evaluate and implement new technologies for formulation and process development or related protein analysis including supervision of students
You contribute to laboratory team capability development, process improvements and `BI safe` concept
You enable and support lab team in detailed planning, execution and interpretation of experiments

Associate, Pharmaceutical Manufacturing Resume Examples & Samples

Assists the Sr. Associate and / or Master Associate with Isolator and equipment set up. This assistance includes tasks such as gathering tools, machine parts, and documents required for such activities. Retrieves components and equipment from aseptic storage
Assists with Isolator and room cleaning in production areas. Will transfer rubbish to the transfer zones and may empty transfer zones of rubbish when required. This includes removal of equipment, room sanitization and disposal of waste according to established safety requirements
Responsible for performing filling operations and assisting in visual inspection operations
Ensures components, materials and supplies are stocked prior to the start of the filling operations

Pharmaceutical Development Technician Resume Examples & Samples

A minimum of 5 years’ direct experience in a heavily regulated (e.g. OSHA, PSM,cGMP) manufacturing and/or research & development environment with a strict adherence to established safety and cGMP rules and regulations performing the activities within the job function
Experience in bulk fine chemicals, bulk API, or petro-chemical organic processing is preferred
A two-year Associates Degree in a Science related discipline is preferred
Proficiency in use of computer programs/systems is essential. Technicians must maintain their skills and knowledge current with the advances in the field of pharmaceutical development
Incumbents may attend internal or external training courses as approved by management
Proficiency in use of computer programs/systems is essential
Technicians must maintain their skills and knowledge current with the advances in the field of pharmaceutical development

Senior Director, Pharmaceutical Development Resume Examples & Samples

Implements comprehensive, compound-specific development strategies and tactics to meet global project needs that incorporates all elements across the drug substance, drug product, analytical, quality and regulatory work space
Leads a high-performing scientific and technical cross functional team of Pharmaceutical Development scientists and engineers
Tracks and reports compound specific expense plans against predefined spending targets
Ensures appropriate technical, scale-up, and production strategies and timelines are in place to meet clinical supply and registration needs, and ensures production, technology transfer, validation and regulatory outcomes, meet or exceeds industry standards
Represent Pharmaceutical Development on the Global Project Teams for assigned compounds
Ensures an effective Target Product Profile is in place which adequately defines the product characteristics and performance expectations to inform pharmaceutical development work
Responsible for ensuring adequate transition plans to transfer knowledge to clinical and commercial manufacturing
Maximizes alignment, cooperation, input, decision making, commitment and synergy, of Pharmaceutical Development team members to ensure their technical contributions, meet and exceed program objectives
Promotes a “One-Team Culture” among scientists and engineers in drug substance, drug product and analytical development, and ensures the Compound Team operates within the mission and values of Pharmaceutical Development and Celgene
Provides sound scientific and technical leadership and advocacy to support the development of robust manufacturing processes and products, integrating current regulatory and industry standards
Communicates effectively and transparently with functional representatives within Pharmaceutical Development, and other stakeholders such as Quality, Toxicology, DMPK, Clinical Pharmacology, Regulatory, Clinical and Commercial Manufacturing, etc.) across the company
Advanced degree in relevant scientific discipline required, Ph.D. is preferred
12 years pharmaceutical development experience with exposure to all stages and aspects of product development
Comprehensive understanding of Drug Product Design and how pharmaceutical development integrates and partners with key functional areas such as Quality, Regulatory, Manufacturing, Clinical, and others
Proven leadership ability to align, motivate and empower team members
Demonstrated ability for critical thinking and innovation
Highly effective at communication, collaboration and negotiation
Accountable for delivery on complex development plans
Ability to understand and communicate risks as well as developing and executing contingency plans for development programs
Ability to manage ambiguity, and make sound scientific and business decisions with limited information (when necessary)
Proven ability to work effectively with cross-functional stakeholders in a complex, changing, environment
Ability to engage and align key stakeholders outside of Pharmaceutical Development and the project team

Pharmaceutical Product Design Integrator Resume Examples & Samples

As a member of the SMDD Design Team, contribute to and/or lead a multidisciplinary group of professionals, scientists and engineers focused on using Human Centered design insights and principles to create value within Lilly's portfolio, including but not limited to
5-7 years of relevant experience in scientific, pharmaceutical and/or health profession related field
Pharmaceutical product development experience preferred
Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position
The qualified candidate will have level appropriate relevant experience in pharmaceutical product development, clinical development, engineering, manufacturing, discovery, business leadership or product design. Demonstrated leadership skills, ability to influence and lead change in a team or organization are required
Demonstrated business acumen and knowledge of those areas needed for development of pharmaceutical products for the drug industry, including formulation and product development, packaging development, manufacturing and global regulatory activities
Creativity, imagination, and ability to transform ideas into effective business processes, products and prototypes
Demonstrated ability to collaborate as an effective team member, influence without positional authority and lead change
Self-motivated with the ability to influence business partners and customers and develop and maintain strong customer focused relationships
Demonstrated strong observational, listening and communication skills
Demonstrated ability to interact and participate with external parties such as consultants and technology providers
Six Sigma Training is considered an advantage
Educational background or experience in Health Professions (e.g. Pharmacy, Nursing, Physician’s Assistant) is an advantage
Background in health sciences or human centered design is an advantage
Experience in developing pharmaceutical dose forms as a formulation scientist, process engineer, or design engineer
Strong knowledge of Design Principles with Focus on Human Centered Design, Human Factors Systems engineering
Experience in Clinical Trial Coordination or support
Outstanding Organizational and Communication (written and verbal) Skills

Pharmaceutical Analytical Chemist Resume Examples & Samples

Evaluating the physical and chemical characteristics of raw materials, intermediates, APIs, and drug products utilizing approved laboratory methods or developing new methods
Executing analytical methods and test procedures in accordance with written processes. Analyzes and report results
Identify and report out-of-trend and out-of-specification results
Reviews current approved analytical protocols and test procedures for process improvement opportunities and/or new or revised regulatory requirements. Develops revised methodology where appropriate
Performs qualitative and quantitative analytical tests utilizing approved protocols and test procedures to support the receipt and release of raw materials, intermediates, APIs and drug products and/or to evaluate unknowns, new materials, and/or new formulations in support of development chemists’ efforts (e.g., identification, characterization, degradation studies)
Performs qualitative and quantitative analytical tests utilizing approved protocols and test procedures to establish and maintain reference and working standards required for the evaluation of APIs and drug products. This includes the characterization, potency, moisture, and purity of reference standards and the preparation, packaging, testing, and inventory maintenance of working standards. Supports vendor contracted to manufacture standards as appropriate
Performs qualitative and quantitative analytical tests utilizing approved protocols and test procedures in support of the Stability Testing Program for APIs and drug products
Documents laboratory activities and maintains laboratory notebook. This notebook is numbered, signed out, and is part of Corporate record retention guidelines
Formalizes analytical methods to be utilized in the evaluation of raw materials, intermediate, APIs, and drug products and creates protocols and test procedures to be followed in future testing
Performs peer review of other analytical research associates’ methods, results, and documentation
Assists with instrument qualification, metrology, and maintenance
Creates, reviews, and/or revises laboratory SOPs when appropriate
Experience developing, revising executing analytical methods
Knowledge and understanding of a variety of analytical techniques including UPLC, GC, UV-Vis Spectrophotometry, and Karl Fischer titration
Experience performing qualitative and quantitative analytical tests
Requires BS/BA in Chemistry
Minimum of 3 years analytical laboratory experience
Familiarity with cGMP regulations and FDA and ICH guidelines

Product Director, Pharmaceutical Resume Examples & Samples

Contribute to the overall evolution of SLF’s Drug Benefits strategy and the products roadmap
Present the Drug Benefits vision at client presentations and industry conferences
Develop strong relations with the various level of governments, as needed, to represent our customers best interests (e.g. contribute, comment and influence proposed legislation)
Sit on industry committees and work with the industry association as applicable
Continue to position SLF as a recognized leader in drug benefits within the insurance industry
Assist our Business Development team with client acquisition and retention, providing them with material and consultation for client presentations
Work with key Industry Stakeholders (e.g. Pharmacy, Manufactures, Wholesalers) to manage current and develop new partnering opportunities
Generate innovative / creative ideas that align to our strategic objectives
Identify and prioritize opportunities for feasibility studies and concepts, evaluating the overall value they can deliver as a basis for prioritization of future product development projects
Accountable for the success of the Drug Benefits offering
Build and influence effective two-way communication with key internal business partners, specifically Business Development, IT, Finance, Legal, Claims/Operations, incorporating their view into the strategy and the product development
University degree in pharmacy
Licensed pharmacist (practicing pharmacist is preferable)
6 - 8 years in a variety of marketing, product development functions, Pharmacy Benefits Management, or other relevant experience

Pharmaceutical Hospital Resume Examples & Samples

Organizes and provides guidance in the business planning process as well as monitoring progress towards individual and district level goals
Identifies opportunities using sales data, insights, and customer needs to effectively
Previous industry management experience (2-3 years)
Previous Hospital/LTC experience preferred
Strong leadership, interpersonal skills and communication agility with various stakeholders
Change agility
Strong business acumen and project management skills
A High School diploma or GED is required
At least 1 year of work experience in a GMP (Good Manufacturing Practice) facility is preferred
At least 1 year work experience in oral solid dosage manufacturing (blending, compression, pan coating, fluid bed or encapsulation manufacturing processes) is preferred
Flexibility to work a non-traditional shift is required
We are hiring for the following shifts

Product Quality Assurance Pharmaceutical Industry Resume Examples & Samples

Bachelor’s degree in Chemistry, Biology, Pharmacy, or related 4 year science degree required
Knowledge, practical application, and understanding of analytical chemistry is necessary to perform the functions of this position
Demonstrated capability for communicating ideas, concepts, and work results effectively to colleagues and supervision
Demonstrated ability to be self-motivated as well as to work collaboratively in a team-based environment is required
Must demonstrate initiative and a willingness to learn
Good working knowledge of advanced laboratory instrumentation and personal computer skills are required
Experience in wet analytical methods and instrumentation techniques preferred; HPLC, UV, GC, IR, AA, TOC, and Dissolution preferred
A working knowledge of organic chemistry, statistics, data processing and good manufacturing practices is desirable
A thorough understanding of National Formulary (NF); United States Pharmacopoeia (USP); and European Pharmacopoeia (EP) testing procedures, as well as, US Pharmaceutical Industry Good Manufacturing Practices (GMP’s), quality control methods and procedures preferred
Competencies required: analytical problem solving, alertness, work within established policies and procedures, commitment to task, decisiveness, effective written and interpretive communication skills, and organization and planning skills
At least 1 year of lab experience preferred
Assigned within the lab: bench chemistry or lab experience preferred

Pharmaceutical Reviewer Resume Examples & Samples

Assistant/Associate Quality Control Lab Analyst provides Quality support to the Incoming Material Supplies Inspection processing and laboratory areas
Will perform activities that support and ensure process quality and data integrity with incoming sampling of raw materials and inspection of primary packing components
The Contractor Quality Analyst will become knowledgeable in Federal and other regulatory agency requirements and cGMPs to assure that all areas in compliance, and will train on and gain competency in activities to support incoming sampling in Classified D and C processing areas and component inspection. Specific responsibilities include but are not limited to the following
Provide on floor support to ensure data integrity and compliance with sampling of raw materials and inspection of primary packaging components
Support regulatory audits Submit Work Orders to maintain compliance within sampling and component facilities Update Supplies Inspection protocols, logbooks, etc. as needed Support Capital Project actions to ensure compliance of new facility
At least one year of relevant post-degree work experience in a laboratory, manufacturing, or quality position. Evidence of good oral and written communication skills, i.e. effective presentation of concepts and ideas, as well as interpersonal and conflict resolution skills
Attention to detail, flexibility and an awareness of production and attendant quality control problems. Basic understanding of GMPs and of regulatory requirements as they apply to the pharmaceutical field or a related area. Preferred Experience and Skills
Experience in quality assurance audits or inspection of vaccine or pharmaceutical manufacturing areas is a strong plus

Janssen R&D Pharmaceutical Development & Manufacturing Sciences Co-op-pa Resume Examples & Samples

Candidates must be enrolled in an accredited college throughout the duration of the co-op
Completion of a minimum of two years towards a BS or pursuing a MS or PhD in Chemical or Biochemical Engineering; Chemistry/Analytical Chemistry; Biology; Biochemistry; Molecular Biology; Biotechnology; Microbiology; Supply Chain Management or related science or engineering disciplines is required
Student must be available from January - June or July - December 2017 and have the ability to work full-time during that time
Extensive PC based skills, including Microsoft Excel, Word, Project and PowerPoint, SAP are preferred (SAP for Supply Chain Management only)
Minimum 3.2 GPA is preferred
Local travel may be required
Students must be legally authorized to work in the United States and not require future sponsorship for employment visa status (e.g. H1-B status) now or in the future.Administration

Pharmaceutical Pricing Fellow Resume Examples & Samples

Prepare concise and well-written reports, memos, proposals, and white papers
Maintain security and confidentiality of all protected health information encountered during performance and other essential functions
Lead meetings, team projects, training on hot topics in the industry, and discuss current topics with clients and inter-professional team
Listen and communicate effectively
Mentor APPE pharmacy rotation students
Collaborate with and understand a wide variety of healthcare professionals, including but not limited to: pharmacists, pharmacy technicians, pharmacy students, other healthcare professionals, educators, and payer drug coverage decision makers
Articulate and know where to access the drug-pricing spectrum—including but not limited to a variety of drug pricing schemes, both on the manufacturer, wholesaler, as well as payer sides of pharmacy. Terms such as AWP, SMAC, NADAC, WAC, ASP, 340B, and who indexes these pricing lists and indices will be explored and mastered
Understand coverage, coding, payment and access for drugs, both in the inpatient and outpatient settings. HCPCS codes, ICD-10 codes, drug databases and clinical and pricing compendia will also be accessed for understanding different strengths of different drug database sources
Exercise leadership and management skills, and learn how to solve problems through data analytics and curating drug information
Practice better writing and editing skills
Complete a research project of publishable quality that is relevant to fellowship activities and interests of the fellow, as coordinated between the fellow, the fellowship director and the pharmacy team
Present research findings and/or submit for publication to a professional journal
Precept P4 pharmacy students on Advanced Practice rotations with student from pharmacy schools via a layered learning model
Participate in training programs to enhance technical, interpersonal and leadership skills
Track and report on new drugs and pipeline drugs utilizing drug compendia, FDA.gov, and other drug information portals
Assist in recruitment and awareness of PPF opportunity in the broader pharmacy community

Pharmaceutical Process Manager Resume Examples & Samples

Collaborate with the PSM Source Team to target pharmaceutical formulations and suppliers, at various stages of the manufacturing process, for detailed process cost analysis
Share knowledge and information with other global donor organizations with a common interest in reducing the cost of lifesaving drugs
Provide thought leadership in the area of market shaping activities through manufacturing process analysis and reverse engineering
Participate in relevant USAID Technical Working Group (TWGs) and other working groups, as appropriate
Visit selected pharmaceutical company manufacturing operations, and work with manufacturing personnel to identify cost savings
Contribute to or write PSM reports, articles and technical documents
Represent PSM at international meetings, as required
Respond to ad hoc requests from USAID/Washington
Minimum 5 years of pharmaceutical manufacturing process analysis experience and a PhD degree in Chemistry or
Minimum 8 years of Pharmaceutical manufacturing process analysis experience and a Master’s degree in Chemistry
Minimum of 3 years’ experience working in pharmaceutical manufacturing operations, with experience writing reports on results of process analysis
Experience improving pharmaceutical manufacturing processes, preferably at the API stage
Experience collaborating with global international development donors on reducing the cost of pharmaceutical products
Experience with giving presentations at major conferences
Experience publishing academic quality studies related to pharmaceutical manufacturing
Strong analytical and statistical aptitude
Experience working in resource constrained countries
A proven ability to work as part of a team and to be self-managing
Proficient in excel, word processing, and presentation applications
Current knowledge of existing developments in the field of laboratory supplies and technology, desired
Working proficiency in French, Spanish and/or Portuguese, desired

Pharmaceutical Manufacturing Technician Resume Examples & Samples

All manufacturing and packaging operations must be completed in full compliance with company SOPs as well as GMPs
Batch manufacturing and packaging documentation as well as all cleaning records and labels must be complete and accurate
Must participate in resolving any non-conformance event
Strict adherence to all OSHA and Company Safety Policies required
Assist in training other technicians and work with R&D Scientists to manufacture product/process development batches as needed
Experience with solid oral manufacturing including fluid bed granulation, blending, compression, pan coating, laser drilling, and tablet imprinting is preferred
Packaging experience also helpful but not required
Familiar with the use and operation of test equipment such as scales, balances, tablet hardness testers, thickness gauges, friabilator and sieve test equipment

Director & Global Head Preclinical Pharmaceutical Developability Resume Examples & Samples

To evaluate the physicochemical properties of Hit-to-Lead to Late-Lead candidates within discovery using the state-of-the-art tools and approaches
To support/develop formulations for early pharmacokinetics studies, pharmacodynamics/efficacy studies, and early toxicity studies including safety pharmacology and tolerability studies
To provide a Biopharmaceutical assessment, which is of critical importance in determining the suitability of a lead candidate for further development and involves many stakeholders
To play a key role in developing experimental protocols, analyzing data and ultimately decision-making. The PDTL should take a proactive role in identifying the right questions and providing the appropriate experimental design using relevant preclinical studies and formulation concepts
In case of unsatisfactory developability properties of a lead candidate, provide input into potential development issues and risk factors and recommend the strategy on how to move forward
Proactively connect and interact with key stakeholders within therapeutic areas, Pharmacokinetics, Toxicology, and PDMS
Responsible for the integrated Developability assessment in close collaboration with the PK representatives and PharmSci Representatives
Provide a complete developability assessment package at the time of Development candidate declaration in order to ensure smooth transition of a small molecule from Discovery into the Early Development portfolio, in terms of formulations suitable for (GLP) toxicology studies, and guidance for the formulation strategy for clinical phase-1 studies
Represent Discovery Sciences at review committees
Keep informed on and invest in innovative screening tools and formulation options to meet the needs of the Discovery and early Development programs, in collaboration with experts within PDMS, academic groups and contract labs
Provide strategic and scientific guidance to a team of scientists (developability representatives, formulators) and lab technicians
Take the scientific and strategic lead in shaping the global Pharmaceutical Developability team to fit with the requirements of the organization, to foster collaboration and synergy across multiple teams, and enhance the scientific expertise
A PhD degree in Pharmaceutical Sciences or Chemistry or proven equal experience, with a strong understanding of Pharmaceutical Development, ADME and Preclinical Safety evaluation
A minimum of 7-10 years of experience as a Pharmaceutical Scientist, with demonstrated experience in developability and formulation strategies, is required
Experience in interpretation of pharmaceutical properties in relation to exposure and toxicology data in drug discovery & development
Organizational, planning, problem solving skills and the leadership skills needed in the completion of deliverables to the discovery Teams
Excellent partnering and decision-making skills
Master the balance between nice-to-have and need-to-have, apply fit-for-purpose approaches to provide scientifically valid assessments
Negotiate and influence decision-making processes, think and manage through issues into resolution, lead scientific discussions
Make fast decisions if needed, but at the same time inclusive and excellent team player
Excellent oral and written communication skills and ability to clearly and concisely present and communicate developability assessment and its impact to various audiences, including medicinal chemists, biologists, preclinical leaders (for both Tox and ADME), and internal boards
Ability to connect and empower people, discover and develop potential and challenge in a positive manner where necessary

Pharmaceutical Account Support Manager Resume Examples & Samples

Pharmaceutical sales background
Project Management Experience Preferred
Experience or interest in Multichannel approach
Ability to plan strategically and logically
Knowledge of the drivers surrounding Community Pharmacy
High level of ability and experience in planning, preparation, and presentation
High-level numeric skills and demonstrates initiative
ABPI Qualified
Degree level education (or equivalent)
Full EU Driving licence (no more than 6 points)
Eligible to work full-time in the UK

Medical / Pharmaceutical Sales Resume Examples & Samples

1) Have the relevant tertiary qualifications from recognized SA institutions i.e. BSc, BCom, BA, etc, (preference is given to life-science qualifications)
2) In rare/special/exceptional circumstances, consideration could be given to a relevant 3 year diploma., i.e. IMM diploma
3) South African citizenship,
4) A valid unendorsed driver's licence and
5) Your own car or access to a vehicle

Account Manager Rx Pharmaceutical Softgel Resume Examples & Samples

Ability to prioritize time on the right opportunities to maximize results
Understands the customer’s decision making processes and identifies each key decision maker’s individual issues and wins
Sets account objectives and establishes a plan for achieving objectives
Cross-sell other Catalent service offerings to softgel customers
Defines alternative solutions of equal attractiveness to Catalent Pharma
Represent the softgel service offering to select Catalent Global Account Teams
Participate in internal sales training efforts, internal process teams, trade show exhibits, and professional associations relevant to softgels and other Catalent service offerings
Research and maintain up-to-date information on the R&D programs of existing and potential softgel customers
Present information about Catalent’s softgel service offering knowledgeably and effectively reflecting the organization’s capability to support development and commercialization of Rx softgel programs
Ability to interact effectively with scientists and technical staff from customers and from the Catalent organization
Communicates in a compelling way and provides proof of value to the customer
Stays informed of and appropriately involved in implementation progress without assuming leadership or implementation management role
Conducts discussions (internally and with customers) and analysis to identify opportunities for innovation
Evaluate overall sales results and trends for assigned portfolio of softgel accounts
Maintain effective communication with Catalent’s scientists, operations staff, project managers, and senior management to ensure that all account management activities are conducted in a coordinated, team-based fashion
Use both structured (e.g., CRM, forms, reporting mechanisms) and unstructured communication (e.g., e-mail, phone calls) to assure that there is a detail-oriented approach to softgel account management with rapid response and follow through to customer inquiries, opportunities, and issues
An advanced scientific degree and/or an MBA degree are preferred
A minimum of 3 years of pharmaceutical contract service sales experience is preferred
Proven track record with new account penetration is required
Excellent oral and written communication and presentation skills are required
Strong computer skills, including Microsoft Word, Excel, and PowerPoint
Ability to work effectively as a member of cross-functional teams is required
Must be willing and able to travel up to 60% to visit clients as well as meet with clients in Catalent's manufacturing facilities in Somerset, NJ and St. Petersburg, FL
This position is not eligible for relocation assistance

Pharmaceutical Regulatory Month Placement Resume Examples & Samples

Our internships will start between mid-June to August 2017 for a duration of 12 months
We are currently advertising multiple internship opportunities within the UK; please apply for the role against which you best meet the qualifications and requirements
Please note that if your skills or experience could be suitable for other internship opportunities we will also consider you for these without you needing to submit a further application
The closing date for applications is the 5th December 2016. However we review all applications on a rolling basis and therefore advise you to apply as soon as possible. We will close our vacancies to new applicants once the requirements have been filled
We are able to offer internships across all GE businesses and as such, our Internship Recruitment Team will provide further information on available industries and locations during the hiring process
Currently studying towards a Lifesciences/Pharmacology related degree – penultimate/final year
Enthusiasm and interest for the functional area applied for
Able to take ownership for projects and work to time limits
Clear communication
Proficient in Microsoft Office
Able to roll up your sleeves and get involved in challenging projects
Well organized administration skills
Inspired and curious
Reliability and dependability

Pharmaceutical Drug Product / LAR Lead Resume Examples & Samples

Lead the GMT Pharma US/LAR Team
Build a team of colleagues that provides project management and technical support appropriate for coordinating
A. GMS US and LAR projects within the internal and external GMS manufacturing network,
B. Regional VMRD projects and BD opportunities
Motivates and lead a group of technical support/project leaders, ensure the team has the appropriate skills, training, equipment and priorities to meet the needs of GMS and to be a valuable asset to Zoetis
Develop and maintain an effective organization; Implement continuous improvement of best practices and standard work (Co-Dev, Launches, Transfers) across projects and the organization to meet company vision and mission
Recognize development needs and create development opportunities within the team. Assess talent needs and identifies talent within the GMT organization
Work with other team leaders on sharing of technical knowledge across the network and encourage others to share knowledge. Contribute to the development of organizational knowledge management processes
Establish and maintain an environment that encourages teamwork, motivation and commitment
Manage appropriate and timely communication on objectives and priorities within the project teams and to stakeholders
Ensuring key project decisions are taken on time to meet the commitments for transfers, new products and life cycle management initiatives
Develop innovative concepts, take appropriate risk to successfully complete projects and guide direct reports on acceptable level of risk taking
Support the development and maintenance of technical support agreements with stakeholders
May lead co-development and/or launch projects
May lead special projects as required by customer and group needs
Support the establishment of the GMT Pharma DP budget, track and ensure alignment
Make decisions on long term objectives, manage projects with cross functional representatives and lead team by influence

Pharmaceutical Production Planner / Scheduler Resume Examples & Samples

Minimum of Bachelors Degree in Management, Business Administration or related disciplines applicable to Supply Chain Management, Information Technology, or Vaccine and Pharmaceutical Manufacturing
Minimum 2 years of relevant experience in Supply Chain, Manufacturing, Materials Management, and/or Marketing. 5 years of experience Preferred
Strong knowledge and practical experience of production, inventory and planning systems currently deployed in Zoetis including but not confined to SAP
Strong knowledge and practical experience in utilizing analytical tools, spreadsheets and databases to develop reports for strategic planning and communication
Proven ability to lead, synchronize and motivate colleagues to meet short and long term objectives
Ability to conceptualize, analyze and implement new methodologies in support of improving customer service, inventory management, and business alignment
Demonstrated ability to function and influence in a team matrix environment and have excellent interpersonal and communication skills
Demonstrated understanding of Right First Time and Lean Manufacturing concepts and principles preferred
APICS training preferred

Pharmaceutical Sales Rep Resume Examples & Samples

 Proactively demonstrate and promote client's products to targeted and non- targeted physicians and healthcare professionals in territory and develop an appropriate territory business plan to influence their prescribing decisions for the appropriate patient
 Develop programs to enhance customer engagement and assist in business plans and goals. Seek and analyze information on competition, market and industry trends and discern how this could impact the business and adapt to changing conditions
 Actively participate in continuous learning and development programs, such as technical updates and professional skills enhancement

Head of Respiratory Pharmaceutical Sciences R&D Resume Examples & Samples

Provides overall strategic, scientific and people leadership and oversight for all aspects of the Pharmaceutical Science R&D group's performance in MGRG in support of Mylan's respiratory product portfollio globally, both internally and with external partner company collaboarations. Formulation, manufacturing (including GMP pilot plant), analytical testing and clinical supply functions totaling more than 100 staff, report to this position. Represents and leads for Mylan as a recognised industry expert on respiratory pharmaceutical science discussions with regulatory agencies and in the wider external environment
Provides overall strategic leadership and direction setting for the MGRG R&D group and sub-functions within the group. Budgetary responsibility for all aspects of MGRG R&D group totaling $40 million per annum
Utilise in depth knowledge of pharmaceutical and material sciences and drug development & industrialisation to set and lead the scientific direction and ensure technical delivery of all aspects of R&D in support of respiratory product filings, approvals and launches
Responsible for leadership, performance management and personal development of over 100 staff within MGRG R&D group. Ensures skills growth and scientific expertise base within own function
Deputises for site leader and fulfills all necessary responsibilities during their absence for the MGRG function at Sandwich site
Broad and deep understanding of Mylan policies and procedures and the ability to implement these at a site level to ensure the safety and compliance of all business activities conducted in MGRG
Represents and leads for Mylan on all pharmaceutical science respiratory topics in the external environment, with regulatory agencies, in key business collaborations and on sensitive due diligence matters
Provides senior leadership (SVP and above) with regular strategic breifings and recommendations on all aspects of MGRG R&D activities
Responsible for all aspects of quality and compliance for the R&D function and staff in MGRG including Pilot Plant manufacturing, the distribution of clinical supplies and the maintenance of the sites IMP and commercial product manufacturing licences
Leads all strategic regulatory discussions on Pharm Sci respiratory product development activities. Provides oversight and approval of all technical documentation prepared and submitted to regulatory authorities in support of respiratory product development activities
Proactive leader of the Mylan Global Respiratory Group leadership team, helping set the strategic direction of the group
Exerts external influence across the industry and on respiratory topics of interest to ensure Mylan's needs and views are represented. Maintains Mylan's external profile as a Centre of Excellence for respiratory product R&D through external presentatiuons and collaborations across industry and with academia
Responsible for strategic recruitment of key R&D and manufacturing respiratory expertise
Proven scientific, technical and regulatory competence and experience with respect to inhaled product development in at least one respiratory dosage form, in one or more of the principal line functions Formulation/Process Development, Analytical Chemistry
Proven experinece to take on larger / more complex roles in business
Proven experience of and demonstrated competence in managing and leading in a range of organisational / operational or national cultures and in managing high intellect individuals
Demonstrable advanced oral and written communication skills to ensure internal and external credibility and influence with senior management, third party partners, regulatory agencies and/or scientific bodies
Demonstrable high level of competence in organisational leadership applying Mylan’s Leadership Expectations of Lead, Learn, Teach, Perform, Attitude
Estimate 10-15% international typical across a 12 month period

Global Client Advisor for Lifesciences & Pharmaceutical Industry Resume Examples & Samples

Contribute to and collaborate on the development of the three year Key Account Strategy as part of the Key Account core team
Work in collaboration with local Oracle resources and teams to execute the Key Account Strategy focused on the truly transformational themes
Understand and be the expert on their customer(s) Business trajectory and transformational goals
Create novel approaches to stimulate transformation in their account(s) utilizing Oracles proven transformational discovery and execution tools and workshop formats
Work extensively with other periphery transformational and value discovery teams within Oracle to run and drive their Transformational Blueprint progress; Oracle Cloud Enterprise Architects, Key Account Marketing, Oracle Insight, Oracle Customer Success, Oracle Consulting, Etc
Knowledge of cloud technologies as part of business re-engineering
Experience in business process design and/ or re-engineering
Detailed knowledge of business process areas such as ERP, HCM, CX, SCM, and common industry processes
Gravitas and confidence based on extensive C-level presentation experience
10+ years experience relevant to this position
Flexible to travel across EMEA region and beyond
Must speak English and (Swiss-)German

Warehouse Pharmaceutical Handler Resume Examples & Samples

Ensure proper packaging, labeling and staging of facility orders
Process, pick, pack, label, and stage all customer orders when needed
Ensure that sufficient quantities of product are in the pick location
Advise inventory analyst of out‐of‐stock or short dated items upon discovery and rotate stock as necessary
Perform physical inventory counts
Meet all department mandated timeframes and deadlines
Previous warehousing, merchandising, or inventory experience, clinical experience preferred
Able to use basic computer skills
Able to work in a fast-paced environment
Must be able to lift and carry 50 pounds
Must be able to work in warehouse temperature environment
6 months-1 year previous warehouse, merchandising, or inventory experience

Pharmaceutical Handler Resume Examples & Samples

Communication – communicates clearly and concisely, verbally and in writing
Interpersonal skills – able to work effectively with other employees, patients and external parties
Policies & Procedures – demonstrates knowledge and understanding of organizational policies, procedures and systems
Basic skills – able to perform basic mathematical calculations, balance and reconcile figures, punctuate properly, spell correctly and transcribe accurately
One year previous Distribution Clerk experience
SMART and WMS experience preferred

International Consultant to Develop M&E System for the Pharmaceutical Sector Resume Examples & Samples

To review existing pharmaceutical M&E setting
To develop and design pharmaceutical M&E system
To design and conduct Training workshop on pharmaceutical M&E
To develop detailed pilot plan
To draw up detailed specifications and TOR for procurement of the approved software for the pharmaceutical M&E system
To submit final report on the whole process and activities under this assignment, and provide recommendations to implement the pharmaceutical M&E system in Sudan
Minimum 5-7 years’ experience is required in monitoring and evaluation of pharmaceutical sector at national and international level
Extensive knowledge of monitoring and evaluation methodologies, indicator developing and reporting particularly in the pharmaceutical sector (proven publications, reports of similar activities)
Experience in designing and implementing country level M&E and HIS trainings
Proven proficiency in the usage of computers and office software packages, experience in handling of web based management system is an asset
Knowledge of UN programmatic processes is needed is an asset

Pharmaceutical Senior Scientist Resume Examples & Samples

Provide technical direction within own area of expertise (GC) within the team whilst independently performing a range of GMP analyses by GC including method development / optimization and validation
Provide high quality customer service at all times by ensuring effective organisation of assigned workload, integrity of analytical data and timely/accurate provision of results
Perform data checking for other members of the team, providing interpretation of results for routine and verification testing, generating certificates of analysis or external interpretive reports
Provide training and coach junior team members in routine activities following pharmacopoeia, client methods and support the interpretation of the resultant data
Liaise with clients, business development and line management to ensure effective communication of project proposals and results
Write and approve SOPs and test methods
Take responsibility for specific project management and/or specific areas of general laboratory/sample administration and assignment of housekeeping tasks as required
Work to the highest standards of safety and quality by ensuring that appropriate COSHHs, risk assessments and SOPs are understood and followed

Associate, Pharmaceutical Manu Resume Examples & Samples

Assists the Sr. Associate and / or Master Associate with assembly and packaging set up. This assistance includes tasks such as gathering tools, machine parts, and documents required for such activities. Retrieves components and equipment from storage
Assists the Sr. and Master Associate with real-time identification and correction of problems. Problems may include, but are not limited to mechanical issues, component issues
Performs all work in accordance with Company Policies and Procedures. All work is documented in controlled documents (batch records, logbooks or SOP attachments) in accordance with SOP. All activities are to be documented in the batch record. All events are to be recorded in the batch record and brought to the attention of the production supervisor for further action
Assists with room cleaning in production areas. Will transfer rubbish to the transfer zones and may empty transfer zones of rubbish when required. This includes removal of equipment, room sanitization and disposal of waste according to established safety requirements
Responsible for following controlled documents to ensure that the equipment identified for operations are used and documented. This includes verification of equipment calibration. Completes log books, as required
Responsible for performing assembly and packaging operations and assisting in visual inspection/filling operations, if required
Ensures components, materials and supplies are stocked prior to the start of the assembly and packaging operations

Senior Pharmaceutical Chemist Resume Examples & Samples

Preparation, review and QC checks of CMC sections of INDs, NDAs, IMPDs and MAAs
Investigation of product complaints and preparation of investigation reports
Preparation and maintenance of Vanda's SOPs for CMC activities
Perform GLP audits of bioanalytical testing laboratories/prepare audit reports
Perform GMP audits of manufacturing, packaging and labeling sites/prepare audit reports
BS or MS in chemistry
3 - 5 years of experience in preparation of CMC documents and performing GMP audits
Knowledge ICH/CTD/FDA/EMA guidelines on preparation of CMC documentation
Knowledge of ICH Q7 and 21 CFR Parts, 11, 58, 210 & 211 and EudraLex GMP regulations
Ability to work effectively and efficiently on multiple projects

Specialist, Pharmaceutical Manufacturing Resume Examples & Samples

Actively participates in the identification and implementation of manufacturing procedure improvements intended to optimize existing or new processes and ensure achievement of regulatory and safety requirements. Updates GMP documentation as required
Ensures work environment meets Boehringer Ingelheim and industry standards. Initiates lean manufacturing techniques in order to actively reduce process and change-over cycle times
Identifies areas for Continuous Process Improvement and applies operational excellence tools to reduce process variability and steadily deliver measurable efficiency gains
Actively participates in troubleshooting and deviation investigations as assigned
Reports findings to management team and team members with recommendations for improvement. Researches new methods or steps in a process, presents findings, and makes recommendations to the team, including developing new and revised Standard Operating Procedures, implementing new equipment and/or developing new processes. Prepares ad hoc reports as requested and maintains/tracks technical and training KPIs. Writes complex explicit documentation for new procedures, as well as for current procedures
Supports the qualification and startup of new equipment in the Fill and Finish area
Develops training manuals and / or on-the-job training materials for new and existing equipment and processes in assigned department. Responsible for development of training materials for new equipment and for review of training materials for current equipment. Completes all required training on time. Is qualified to conduct on the job training in packaging. Assists with drafting of revisions to and creation of new SOP’s. May require “on the job training” certification

Pharmaceutical Packaging Engineer Resume Examples & Samples

Coordinates all aspects of labeling and packaging for all commercial programs, including Purchase Orders of production and components, Quality System associated documentation, and/or any pertinent documents
Ensures that product manufacture occurs in compliance with cGMP and applicable regulations
Forms relationships with technical and operational colleagues to effectively collaborate with other departments and contractors
Supports Manager of Commercial Pack & Label, as needed
Participates in continuous improvements, system implementations and/or to reduce cycle times and improve efficiencies for area
Ensures off-site inspections, testing, and shipping/packaging is done according to guidelines and specifications
Provides regulatory filing support to IND, BLA, MAA, etc
Maintains metrics to analyze department activities, workload and performance
Travel extensively (75%) to contractors for overview of operations as needed
Ability to interprets and communicate information
Ability to effectively communicate with co-workers and customers
Ability to work independently or on a team
Ability to prioritize, manage multiple tasks, and meet deadlines
Ability to organize and maintain data or information
Ability to interpret and apply cGMPs, USP, regulatory requirements and industry best practices
Ability to understand and manage project plans, budgets and schedules
Excellent interpersonal and leadership skills and abilities
Solid team player able to function within a team based organization
Expertise in filled drug product packaging process technology
Expertise in package component artwork and specification process development
Working knowledge of project management software and continuous improvement methodology
BS/BA degree in business administration or life sciences required
3+ years’ experience in dealing with Contract Manufacturers or Suppliers or transferable experience; OPM/MRP experience desired
Pharmaceutical package engineering and project management experience preferred
Title level (Associate Specialist, Specialist, or Sr. Specialist) will be determined based on skills and experience

Pharmaceutical Technology & Development Graduate Programme Resume Examples & Samples

High-achieving, technically expert graduates in chemistry, physics, chemical or mechanical engineering, pharmacy or related subjects who have completed their first degree or Masters in 2015/16, or are due to graduate by September 2017 with a 2:1 or higher or equivalent grading
Innovative thinkers whose enthusiasm matches their scientific expertise
Confidence and desire to tackle new challenges and work situations with ease
Energy and motivation to be part of a team that believes collaboration is key to meeting the unmet needs of patients

Pharmaceutical Sales Specialist Resume Examples & Samples

This position is for a Diabetes Specialty Sales Representative within our Diabetes Franchise
Candidates must be able to understand and apply knowledge of health care industry trends, applicable laws and regulations, market conditions, and the market access environment (including but not limited to pharmaco-economics and the payer/reimbursement landscape) and analyze these factors in the development of territory business plans and in daily execution of sales calls within compliance guidelines
Develops and implements territory business plans centered on Endocrinologists and other Diabetes specialty customers. These plans will focus on performance and execution impacts that properly identify and prioritize activities to accomplish short and long term business goals
Demonstrates a deep, clear and thorough understanding of the Diabetes disease state, Diabetes products and relevant competitor products, including their mechanisms of action, indications, efficacy, and safety, etc
Demonstrates highly effective territory management skills and exemplary selling competencies
Collaborates with territory matrix team on identifying business opportunities and developing appropriate tactics and strategies
Fosters team effectiveness and accomplishment of shared goals by sharing knowledge, experience, and information
Drives market share growth and maximizes sales performance within the indicated use and for the approved patients
Minimum of 5 years of Pharmaceutical Sales Representative experience required; the last 3 years having been in a Diabetes Sales Role, specifically with building relationships and sales with Endocrinologists
Diabetes specialty marketplace experience preferred or other demonstrated Diabetes therapeutic experience preferred in addition to the requirements listed above
Demonstrated skills at building and maintaining professional relationships with key customers, office staff and others in the customer influence network
Evidence of strong established relationships with local endocrinology specialists preferred
Demonstrates comfort with technology and uses technology to increase the efficiency and effectiveness of work processes and sales calls
Demonstrated strong business analytics ability to analyze data as well as develop, execute and adjust business plans
Demonstrated ability to work in matrix teams
Demonstrated track record of developing self to drive and enhance performance

Pharmaceutical Sales Specialist CV East Resume Examples & Samples

Drive sales performance and ensure sales forecasts and assigned budgets meet or exceed therapeutic and territory expectations
Provide special education to healthcare providers through appropriate programs that fall within AstraZeneca's ethical guidelines
Work with other Pharmaceutical Sales Specialists around common objectives to coordinate selling efforts
Provide timely and competent administrative management of work hours, sales call data, customer objectives, communication responses, synchronization, sample and expense reporting
Call on physicians in hospital settings, and residency and fellowship programs within a defined geographic territory
Responsible for positioning AstraZeneca as a leader in Oncology commitment through development of long term relationships with Key Customers
Work with RAD and District Sales Managers to develop and direct sales strategies at key accounts assigned in the territory
Develop and direct sales strategies at key accounts assigned in the territory
Develop and implement clinical sales presentations to groups of healthcare personnel during medical meetings, and the general public in health fairs and support groups
Experience selling and knowledge of Oncology products or diseases preferred. Breast and lung cancer drug sales experience strongly preferred for Oncology positions
Demonstrated clinical selling skills
Demonstrated ability to manage PREP budget and to work through the PRA process
Knowledge of medical office equipment, territory management direct and in-direct sales processes
Possess excellent written and verbal communications skills, and presentation skills
Business administration skills
Laptop computer skills
Managed Care knowledge including prior authorization successes, demonstrated understanding of managed care contracting
Proven ability to understand, internalize, and routinely present challenging scientific information
Effective communication abilities to include strong group presentation skills
Ability to freely accept, implement, and exchange best practices
Achieve and exceed sales goals while managing a budget using good judgment
Regularly use a variety of analytical tools to understand and evaluate the business in order to best determine how to accomplish sales objectives
Develop and maintain in-depth knowledge of market, demographic, and managed care information relative to assigned sales territory
Be results oriented with demonstrated time

Pharmaceutical Sales Specialist CV CCS Resume Examples & Samples

Responsible for developing /positioning AstraZeneca as a leader through development of long term relationships with key Interventional Cardiologists and with key accounts as appropriate
Develop superior product and disease state knowledge and effectively educate and engage healthcare professionals in dialogue about clinical evidence, approved indications, and product efficacy/safety profiles to support on-label prescribing for appropriate patients
Work with Regional Sales Director, Institutional Director and District Sales Manager to develop a local strategy and business plan to generate recognizable increases of sales in territory
Work within a framework of AstraZeneca's Leadership Capabilities
Knowledge of the medical, healthcare or pharmacy industry and skills in clinical selling are preferred, but not required
Leadership, self--motivation and initiative
Demonstrated technical aptitude and computer skills are essential management skills
At least two years of documented, full-time, successful pharmaceutical sales
Strong clinical skill, and sales ability
Internal candidate must be Career Ladder Level 2 and above
Four or more years in AZ Pharmaceutical Sales (Internal Only), or related sales experience, preferably in the anti-platelet, cardiovascular, gastrointestinal, and respiratory markets
Experience in working with interventional cardiologist

Pharmaceutical Sales Specialist RST Pss-cleveland E Resume Examples & Samples

Work with Regional Sales Director and District Sales Manager to develop a local strategy and business plan to generate recognizable increases of sales in territory
Respiratory specialty marketplace experience preferred or other demonstrated Respiratory therapeutic experience preferred in addition to the requirements listed above
Demonstrated strong capability in account management and proven sales performance track record
Demonstrated understanding of the business drivers, dynamics, regulations and market access environment within the pharmaceutical industry
Effectively use active listening, probing and other selling skills to enhance communication and build and influence key customers

Pharmaceutical Sales Specialist Immuno Resume Examples & Samples

At least two years of documented, successful pharmaceutical sales, or at the discretion of those involved in the hiring process, related sales to physicians and hospitals such as medical equipment
Experience selling and knowledge of Oncology products or diseases preferred
History of building and influencing customer relationships, and goal achievement
Demonstrated clinical selling skills and business acumen in complex selling environment
Responsible for selling, maintaining and documenting all sales activities for the AstraZeneca Oncology portfolio of products to physicians in private practice, in group practices, in hospital settings, and Oncology residency and fellowship programs within a defined geographic territory
Maintain a high level of clinical expertise by consistently utilizing all available medical information resources
Develop and implement clinical sales presentations to groups of healthcare personnel
Maximize key physician contact by networking within accounts and at all medical meetings

Security Account Manager for Pharmaceutical Giant Resume Examples & Samples

Supervise the day to day security operations of an assigned Client Site
Build, improve and maintain effective relationships with both client and employees
Ensure all required reporting and contract compliance requirements are met
Communicate staffing needs via Requisition Form; assist recruiters in identifying, interviewing and hiring quality candidates
Develop staff in both technical and professional skills through performance management (coaching, counseling, disciplining, MSO training, annual formal performance evaluations, recognition, etc.)
Assure that employee grievances are heard and resolved (with help from appropriate support employees, as required) and that personnel records are updated and accurate (Change of Status forms, rosters, etc.)
Assure communication of policies, company announcements and job openings through a consistently updated READ file at each site
Meet all contractual scheduled hours with a minimum of unbilled overtime
Coordinate and/or conduct site-specific OJT, client-specific training, and annual refresher training for security personnel, as well as meet AlliedBarton’s corporate training standards
Manage uniforms, equipment, supplies and vehicles utilized at the account(s), maintaining appropriate inventories and maintenance checklists
Take a proactive role in communicating with the client and meeting his needs; meet with regularly, listen to issues, provide security and technical expertise and solutions. Ensure complete customer satisfaction
Capably utilize WinTeam for scheduling and billing, and to produce reports (such as Scheduling Activity, invoice Aging by tiers, Training Summary and Training Detail reports) that require interpretation and action for effective business management
Enforce AlliedBarton policies as outlined in the handbooks, executive memos and on the portal
Four year degree in Criminal Justice, Business Administration or related field
Outstanding interpersonal and communications skills required
Ability to manage multiple priorities, complex situations, a diverse team of employees and client requirements on an ongoing basis

Senior Business Analyst Pharmaceutical Industry Resume Examples & Samples

Develop/Modify User Acceptance Test (UAT) Scripts, Execute UAT Scripts and prepare User Acceptance Reports for LSH Implementations and Upgrades as per internal System Validation SOP’s
Develop/Modify System Tests Scripts, Execute System Scripts and Support the execution of System Test Reports for the LSH environments as per internal System Validation SOP’s
Support IT and Business in infrastructure and the LSH application upgrade
Provide Subject Matter Expert (SME) support in the Clinical Data Flow activities from the Systems perspective and provide recommendation
Support and provide recommendations in conducting Proof of Concept to minimize system downtime during the migration process of LSH system
Work in close collaboration with internal IT organization in support of LSH upgrades and updates
Support the Internal Business Functions

Pharmaceutical Alliances Operations Manager Resume Examples & Samples

Ability to work in a multi-functional and multi-cultural environment and awareness of cultural sensitivities
Ability to build effective internal collaborations with UCB colleagues
Ability to coach and support alliance managers and IT systems users (ie multiple individuals with varying styles and needs)
Dedication to providing work of an excellent quality, focusing on attention to detail and task completion
Excellent planning and organizational skills to ensure effective and timely output in an independent way
Experience with various IT systems, ideally including CRM and SAP
Ability to handle a number or diverse projects and people at any one time is essential
Deal appropriately with confidential and sensitive matters
Ability to solve conflicts and to seek help for this if needed
Team player enjoying coordinating group activities
Willingness to learn, open and adaptable personality
Should be open to feedback and proactively seek it
Anticipate potential issues and resolve them before they transform into problems
Fully motivated to be a part of a community network and contribute towards it
Language skills : French and/or Dutch in addition would be a plus
Two or more years Hospital selling experience
Experience working in the Cath Laboratory
Experience influencing formulary decisions
Bachelor's Degree or equivalent
Five years of pharmaceutical sales representative experience with the last 3 years in a Diabetes sales role
Account management experience
Preferred Diabetes Sales experience
Demonstrated effective leadership, organizational and communication skills

Pharmaceutical Auditor Resume Examples & Samples

MS in Chemistry preferred, BS in Chemistry
A minimum of 5 yeas experience in a pharmaceutical company within Quality Assurance/Quality Control
Two (2) years of experience reviewing analytical data
Proven knowledge of QC lab test procedures including analytical method transfer, method validation, raw material analysis, finished products and stability testing procedures

Head of Pharmaceutical Development Resume Examples & Samples

Develop and oversee implementation of all activities related to Pharmaceutical Product development for products in the PTDU portfolio
Provide strategic leadership for the formulations & stability efforts to support early and late stage clinical studies, commercial launch and significant post-market modifications. This includes
Developing robust formulations and manufacturing processes for all pipeline products in PTDU portfolio
Develop new technologies & innovative drug delivery approaches enabling future products, such as ocular products, co-formulated products and sustained release products
Identify, prioritize & oversee DP processing technology development efforts in line with mid to long term business objectives
Oversee execution of drug product process characterization and validation programs in preparation for licensure, with a focus on continuous improvement and productivity
Oversee equipment development and qualification activities
Provide leadership direction for production of material in Genentech’s clinical & commercial manufacturing facilities, transferring formulation & technical knowledge and processes to commercial sites and providing ongoing support where appropriate
Ensure sufficient expertise is available to support all Drug Product programs
Provide senior level contributions to the development of the PTD business strategy, culture and capability
Take personal accountability to Sponsor PTD initiatives and projects as requested by PTD leadership
Implement CMC Productivity initiatives and cultivate an organizational culture that is agile, lean, innovative and encourages smart risk taking
Provide leadership and development of staff with strong focus on continuous improvement, performance management and career development
Foster teamwork among global and local colleagues
Evidence of strong established relationships with local endocrinology specialists
Understanding of the business drivers, dynamics, regulations and market access environment within the pharmaceutical industry
Skills at building and maintaining professional relationships with key customers, office staff and others in the customer influence network
Strong business analytics to analyze data as well as develop, execute and adjust business plans
Ability to work in matrix teams

Director, Pharmaceutical Sterile Technology Resume Examples & Samples

Conduct and/or oversee laboratory research in process development for pharmaceutical sterile products
Evaluate, recommend, and oversee contract research and manufacturing organizations capable of providing the technical services required
Direct and coordinate process optimization of development formulations
Direct and participate in technology transfer and validation efforts at commercial manufacturing sites
Provide technical support of commercial products to ensure adequate supply at all times
Coordinate project activities with other internal functions through the Product Development Teams
Review of CMC documentation for US and ROW submissions
Build and maintain a strong working relationship with colleagues in Analytical Research, Project Management, Quality Assurance, and Regulatory Affairs
Prepare and review CMC submission documents
Interface with Regulatory Authorities pre and post submission as required to support global filings
Participate in due diligence activities as required
Ph.D. in a relevant discipline, with ten (10) years experience in sterile pharmaceutical dosage form technology/development, or M.S. with fifteen (15) years experience, or B.S. with twenty (20) years experience
Hands-on experience in sterile pharmaceutical dosage formulation and production
Expertise with sterile pharmaceutical processing equipment, including ability to set-up, operate, and trouble shoot equipment
Ability to work with multiple disciplines within the organization, including but not limited to Analytical Research, Marketing, Project Management, Quality Assurance, Regulatory Affairs
Management of contract organizations
Thorough understanding of QC sampling, testing, and interpretation of analytical results
Time management and the ability to multitask, as multiple projects will be operational at the same time
Strong knowledge of cGMP
Domestic and international travel will be required
Maintain a high level of product knowledge, policies, procedures, contacts, and the pharmaceutical industry; continual learning & training as required
Ensure timely and appropriate communication occurs with sales professionals in the field
Minimum of 2 years of sales experience in an office/call center environment required
Experience contacting or detailing Physicians or Healthcare Professionals strongly preferred
Demonstrated ability to learn, retain, and articulate technical and scientific-product related information, and provide unscripted responses on appropriate subject matter
Superior rapport and relationship building skills

Pharmaceutical & Life Science Commercial Senior Associate Resume Examples & Samples

Define the desired customer experience through customer and market insight
Identify and remedy billing and other performance issues that lead to customer dissatisfaction
Writing, communicating, facilitating, and presenting cogently to and/or for all levels of industry audiences, clients and internal staff and management, including utilizing MS PowerPoint and Adobe Creative Suite
Developing mobile applications for a payer or provider

Sterile Pharmaceutical Manufacturing Supervisor Resume Examples & Samples

Supervise multi-skilled personnel as assigned, to ensure that performance meets established safety, quality/Good Manufacturing Practices (cGMP), quantity and cost standards
Manage, coordinate and directly supervise employees including coaching, counseling, performance reviews and feedback/initiating corrective action as needed, in a timely fashion
Collaborate with other area supervision and Human Resources in ensuring consistency in situations requiring corrective action with employees
Provide leadership and support to production and non-exempt production personnel in solving technical problems or contacting other resources as appropriate to solve problems
Ensure compliance of local, state and federal regulations and guidelines (e.g., Good Manufacturing Practices (CGMP), Occupational Safety and Health Administration (OSHA), Environmental Protection Agency (EPA), etc.). Ensure SOPs for areas of responsibility are updated, accurate, and complete
Ensure formal and informal training occurs in employee technical skill development as well as other training initiatives including safety, CGMP, teamwork, etc
Support the Head of Manufacturing in the timely completion of assigned projects, including participating in the design and development of new packaging/production materials, equipment and packages
Participate in cost reduction programs with respect to waste and other inefficiencies
Perform other supervision duties and responsibilities as assigned
Position is for 3rd Shift, Sunday through Friday (10:00pm to 6:30am)
Bachelor’s degree and at least 4 years’ production supervisory experience in a government regulated industry using QA procedures (FDA, pharmaceutical industry preferred)
If no degree, but have 5 years’ supervisory/leadership GMP packaging/liquids experience, must commit to start/continue college degree / certification program
Master's degree & 2 years’ experience listed above or PhD and 1 year experience listed above may be considered
Strong personal computer skills required; experience with windows environment, Microsoft WORD and Excel preferred. Knowledge of automated Materials Requirement Planning (i.e. MES) system preferred
Demonstrated ability to communicate positively with personnel at all levels
Demonstrated ability to collaborate with others in cross-functional settings
Proven organizational, analytical and problem solving skills are required to appropriately balance short-term business demands
3rd Shift Position Sunday through Friday (10:00pm to 6:30am)

Pharmaceutical Production Manager Resume Examples & Samples

3 – 5 years pharmaceutical / FDA regulated production, new product development, or API manufacturing required
1-2 years production management / supervision experience required
6+ years pharmaceutical / FDA regulated production, new product development, or API manufacturing preferred
3+ years production management / supervision experience preferred

Associate Scientific Director Pharmaceutical Sciences Program Management Resume Examples & Samples

Must have the maturity to utilize scientific and technical knowledge to provide unique business solutions
Experience must be in a scientific discipline with expert knowledge of pharmaceutical development, including an understanding of current laboratory techniques, instrumentation, problem solving techniques, process engineering and manufacturing development, and statistics used in experimental work
Must demonstrate knowledge of several allied fields such as chemical engineering, analytical/organic/physical chemistry, process engineering, pharmaceutics, quality assurance and/or regulatory affairs. Fundamental understanding in DMPK, Pharmacology and Toxicology
Extensive knowledge of current Good Manufacturing Practices (cGMP), ICH Guidelines, other pertinent national regulations, compendial requirements and communicating with regulatory agencies
Must have experience in global regulatory submission requirements and processes
Leadership- develops and uses knowledge and interpersonal skills to influence and guide internal and external stakeholders towards the accomplishment of program and cross-divisional goals and objectives; adapts well to varied team dynamics and manages others team members in a respectful manner
Risk Management – ability to identify/mitigate technical, budgetary, and schedule risks to multiple programs and propose appropriate risk response strategies. Ability to identify gaps in PS technology/trends and influence change/improvements to affected areas/processes
Communication– ability to expresses one’s self clearly and concisely to key stakeholders and functional management; documents issues and/or concerns concisely and comprehensively; adjusts style, language and/or terminology appropriate for the audience. Can represent PS viewpoint at divisional level
Resource Management – Ability to anticipate and manage internal and external resource needs (people, information, technologies, time, and capital)
Willingness to travel to various meetings or client sites, including overnight trips. Some international travel may be required
Requires approximately 10-30 % travel

Women s Health Pharmaceutical Territory Manager Resume Examples & Samples

BA/BS Required
3+ years pharmaceutical sales experience with proven track record of success
Required residence in territory geography
Knowledge of Women’s Healthcare market preferred
Demonstrated competency with studies/clinical reprints and other third-party proof sources
Proven PC skills required (Microsoft tools)
Ability to read, analyze and interpret general business trade journals, professional journals, and financial reports
History of building a network of customers and industry contacts, including KOLs and speakers
Responsible for continued knowledge development and market trend analysis
Proven track record of achieving annual target goals
Ability to work independently and without direct daily supervision
Skilled in strategic selling with a desire to assist others to achieve success
Excellent verbal and written communication skills necessary
Strong presentation skills with respect to products and tertitory
Valid driver’s license to travel to customer locations
Some overnight travel required

Pharmaceutical Opr Resume Examples & Samples

Work with the other pharmaceutical operators and supervisors in assigned area to establish priorities and meet deadlines. Meet the production schedules outlined by team and/or Supervision
Ensure product quality by performing in-process checks, complying with cGMPs, being alert for unacceptable quality of incoming and outgoing materials, initiating quality improvements, and participating on quality improvement projects; Communicate quality and other non-compliance issues to supervision in a timely manner
Review and approve work output for team members by using validated methods
Perform work, on personal computer (i.e., Business Operating Systems, read and respond to electronic mail in a timely manner, Microsoft Software, etc); Complete, maintain, and update production documentation (both electronic and paper) to perform material movements, material take-outs and yield determinations by following SOPs and utilizing systems as required such as Systems/Applications/Products (SAP), Manufacturing Execution Systems (MES), Electronic Batch Records (EBRs), etc
Operate motorized and non-motorized material handling equipment for assigned stocking operations as well as stand up and sit down forktrucks as needed
Inform department Administrative Assistant when to order supplies as needed
Coordinate the utilization of outside contractors and vendors as needed
Manufacturing experience

Pharmaceutical Operator Resume Examples & Samples

Ensure safe work environment by following all safety procedures, workplace standards and company guidelines, and ergonomic rules, including proper use of personal protective equipment (PPE), standard operating procedures (SOPs) applying to a particular process or area, Current Good Manufacturing Practices (cGMPs), Occupational Safety and Health Administration requirements (OSHA), Lockout Tagout
Dispense components, operate, clean, set-up, changeover and maintain equipment and rooms to manufacture products. Clean and maintain process equipment which may include, but not limited to tanks, filler, pumps, blenders, mills, presses, coating pans, etc
Assist with technical troubleshooting and preventive maintenance tasks as needed and trained. Take action to safely reduce equipment setup and changeover times; Initiate and establish equipment operating parameters to maximize production, while meeting all product specifications
Accurately record on the appropriate documents the process/manufacturing steps, production results, equipment in-process checks, samplings, cleanings, ingredients used, and any other required cGMP information. Maintain daily production sheets and time sheets for team
Take ownership of training and learning to develop high performance competencies such as technical skills, communication skills, and skills to build a team-oriented culture (i.e. take ownership of training records for self-development and submit to supervision in timely manner, training team members, motivating and supporting team members, sharing knowledge to continuously improve the process, etc.)
Cross train and train other pharmaceutical operators on equipment and processes as needed
Participate in on-going medical surveillance programs as required
Perform other duties as trained and assigned
Must be physically able to operate a forklift truck; forklift truck experience

National Account Manager Pharmaceutical Hub-telecommute Resume Examples & Samples

Develops Hub strategy
Demonstrates technical selling skills and BriovaRx service model expertise
Collaborates with pharmacy operations team to ensure superior customer service
Analyzes and summarizes data and trends
Routinely communicates with centralized marketing team regarding resources, competitive activity, etc
Interfaces with biopharmaceutical manufacturers to highlight BriovaRx's service excellence
Builds business relationships with health care professionals
Updates job knowledge by participating in educational opportunities; reading professional publications; participating in professional organizations
Maintains accurate records of all sales activities including salesforce.com
Demonstrates ability to effectively interact and cooperate with all company employees
Complies with all company and government policies, regulations and business ethics codes and ensures they are communicated and implemented within the team
Bachelors of Science Degree
2+ years of Specialty Pharmacy experience
5+ years of healthcare related sales
Willingness to travel a minimum of 50%
Pharmacy Degree
Experience in HCV, Autoimmune, Oncology and/or Multiple Sclerosis

Global Client Advisor for Life Sciences & Pharmaceutical Industry Resume Examples & Samples

Proactively drive business transformation discussions with very senior business people in the customer in order to own and execute full transformational engagements, (Transformational BluePrints), underpinned by Oracle’s tools, solutions and technologies
Create Industry focused transformational execution patterns that can be re-used by colleagues, (Transformational BluePrint Patterns)
Collaborate with Client Advisor colleagues globally in order to share best practices and customer insight within their industry communities
Broad business-wide industry expertise and knowledge
Experience driving business transformations underpinned by systems and technology
Track record performing discovery for digital transformations as well as executing digital strategies
Some knowledge of Oracle technologies, specifically it’s cloud stack
Must speak English and (Swiss-)German, French is a plus

Senior Pharmaceutical Batch Engineer Resume Examples & Samples

Hands on experience on pharmacy batch project. Did documentation preparing (complied with GaMP5 and ICH Q9 Quality Risk Management)
Knowledge on pharmacy process (familiar with one or two typical process)
Understand pharmacy industry control project requirement
Understand S88 standard, FDA 21 CFR 11
Minimum 5 years of pharmaceutical batch project or Pharmacy factory DCS system maintenance experience
Computer science fundamentals (OOPS, Operating System, Data Structure, Office)
Knowledge on Microsoft SQL Server 2000 / 2005 / 2008, VB,VC++ preferred
Willing to study & Learn new technologies on demand through websites and implement the same as per the project requirement in Batch project domain
Knowledge on testing methods will be an added advantage

Group Leader, Pharmaceutical Development Resume Examples & Samples

Develop and execute manufacturing work plans/schedules for self and team, using customer milestones and Division/site performance standards and metrics
Independently authors and approves technical documents, such as protocols, technical reports, test methods and operating procedures
Review technical documents for accuracy, thoroughness and regulatory compliance
Trains, coaches or mentors others on technical, personal development or business issues
Supervises technical staff, including work assignments and performance and development management
Responsible as project director on multiple projects, with responsibility for project outcome and customer interaction, including developing customer relationship to grow the business
Identifies and independently drives department level improvements
Identify and recommend business strategies for multiple customers across multiple company sites
Manages professional employees and/or supervisors
Is accountable for the performance and results of a team within own discipline
Adapts departmental plans and priorities to address resource and operational challenges
Decisions are guided by policies, procedures and business plan; receives guidance from manager
Provides technical guidance to employees, colleagues and/or customers
Uses leading-edge knowledge of principles, concepts and practices and/or techniques to lead complex projects within a department/ group/team that may involve related departments/groups/ teams
Applies technical, functional, business and/or industry knowledge to design experiments/projects
Provide scientific consultation to the department/ discipline/group
Actively contributes to the strategic direction of the department/ group by recommending expansion or curtailment of investigations on the basis of experimental results or scientific information
Maintain high quality documentation in accordance with applicable regulatory guidance and Site SOPs
Experienced in most aspects of drug development and lifecycle support, and able to develop useful strategies and tactics to meet regulatory milestones
Has substantial breadth/depth of technical acumen in multiple techniques with significant expertise in one or more techniques and can understand their application in context of pharmaceutical services offerings
Capable of rapid learning of multiple unfamiliar principles or techniques with minimum training
Is able to lead difficult discussions with customers and drive the conversation to an acceptable resolution
Recognized by internal and external customers and direct reports as a subject matter expert with high personal credibility
Can assess training needs and formulate development plans for direct reports
Works directly with Business Development to win new business (conference calls, new customer meetings, some travel)
Ability to interpret, provide and manage a variety of instructions furnished in written, oral, diagram, or schedule form across multiple work groups and departments
Understands the details of regulatory CMC filing package and the analytical and formulation documentation required therein. Has the ability to write and review documents for regulatory filings
May publish or present externally

Associate Pharmaceutical Buyer Resume Examples & Samples

Work with the pharmacy to establish product/service requirements. Order pharmaceuticals and supplies for the pharmacy
Maintain all backorder information. Research and maintain statistics of all items missing from the pharmacy floor
Compile monthly reports on performance against targets and monitor, track and report pharmacy inventory monthly
Special projects as assigned
3 – 5 years of relevant work experience
Strong organizational skills and problem solving skills; Strong math skills; Demonstrated ability to meet multiple deadlines and manage heavy workload; Excellent verbal and written communication skills; Contracting experience preferred
Prior experience working in a pharmaceutical, biotech or food manufacturing environment (regulated by GMP standards and requirements) is preferred; with specific experience in oral solid dosage manufacturing (blending, compression, pancoating, fluid bed or encapsulation manufacturing processes)
Knowledge/Skills Requirements: (List unique knowledge skills, or problem-solving requirements)
Technician in Training & Secondary Qualified Technician
Work in a safe manner
Legible hand writing skills
Primary Qualified Technician
All requirements listed above for both Technician in Training and Secondary Qualified Technician
Technical skills/trouble shooting skills
Physical Requirements and Safety Considerations of the Position
Work Schedule: Shifts of 8 or 12 hours in duration
Encapsulation Only - Individual must also be able to pass standardized color plate performance (HRR: PSEUDOISOCHROMATIC PLATES) and have corrected or uncorrected visual acuity of 20/30 near vision
Essential Physical Job Tasks
Manipulation of drums to and from 6-inch pallets
Drum weight <10kg. (Empty) to 150kg (max. full weight) up to 30 times per shift
Maneuvering of drums in lab consisting of rolling, scooting, pushing and pulling (up to 80 lbs. of force)
Utilization of scoops and other hand held implements
Lifting boxes and/or containers up to 40 lbs. (18.2 kg) from waist to chest height
Loading product of various amounts of completion to counters and quality control devices
Push and pull ingredient canisters
Cleaning of Lab and equipment
Utilizing hand held brushes, wands, hoses, and other cleaning utensils
Transport of materials to and from designated lab space
Use of various job task dependent tools and work saver equipment including pallet jacks
Safety Considerations
Must wear safety glasses, or specified eye protection, in all designated areas
Must follow any applicable plant safety requirements
Must be fit-tested, trained and capable of wearing air purifying respirator
Must be trained in plant hazardous material procedures
Must use approved fall prevention devices when performing elevated tasks
Must be capable of wearing steel-toed safety shoes for 8 to 12 hours a day, depending on duration of the shift
Environmental Conditions
Working conditions will be Heating Ventilation and Air Conditioned controlled

Head Pharmaceutical Development Small Molecules Resume Examples & Samples

Provide vision and leadership to establish clear goals and expectations of the department in alignment with portfolio and corporate objectives. Is a member of the Small Molecule Development leadership team
Develop, implement, and monitor practices, policies and strategies for the department to support the small molecule portfolio. Ensure that projects receive necessary resources and scientific support. Efficiently partner with other departments locally and globally
Develop and implement short, mid, and long term strategies to ensure scientific excellence, state-of-the-art technologies, and regulatory compliance. Ensure balanced investments (internal and external collaborations) for formulation development technologies to enable the Roche portfolio
Initiate and promote technical relationships to develop technical networking in maintaining knowledge of industry practices and communicate and/or applies new advances in the field. Influence evolving regulatory standards through participation in professional and trade organizations
Ensure and monitor laboratory compliance with current Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs) and regulatory requirements for development and line-extension projects. Ensure technical training of personnel is current and that laboratories are using current and state-of-the-art methods in accord with industry and regulatory standards. Ensure proper qualification, validation, and maintenance of all equipment
Provide professional development opportunities for all personnel. Manage performance and provide opportunities for personnel/professional growth
Manage a portfolio of projects and apply broad knowledge of drug product development to decision making and problem solving while managing expense, capital, and grant budgets to ensure smooth operation of the department

Postdoctoral Research Fellow Pharmaceutical Sciences Resume Examples & Samples

Support the design and development of nanoparticle and extended release formulations through experimental design, planning, execution and data interpretation
Support physical, chemical and biophysical characterization of formulations
Support in vitro cellular assays and in vivo testing in preclinical animal models
Present scientific results at meetings and in technical reports/publications, internally and externally
Demonstrated ability to conduct independent research and solve scientific problems in a highly collaborative environment
Be energetic, enthusiastic and self-motivated, with a strong desire to learn and contribute
Strong scientific acumen, with ability to solve problems of medium/high complexity via independent planning, design, execution and interpretation of experiments
Academic experience in non-conventional injectable drug delivery technologies, including lipid- and polymeric nanoparticles, nano- and micro-suspensions and depots
Academic experience in cell-based assays or in vivo models
Strong history of publication in peer-reviewed journals

Chemical & Pharmaceutical Market Sector Leader Resume Examples & Samples

Provide market sector leadership and leads the sales planning process for the market within the Region
Serve as regional representative to the national market sector team, bridging national key account priorities to regional opportunities, maximizing business generation from key accounts within the region
Lead business development teams to define capture strategies and direct the most important regional pursuits, especially for key accounts and major projects within the regional market sector
Develop overall regional market growth strategies, which articulate market trends/drivers and recommended priorities to successfully invest and grow, consistent with the business line’s, the region’s, and AECOM’s overall growth objectives
Coordinate the activities of assigned Key Account Managers, including local Key Account Managers, to maximize business for key accounts within the regional market, especially by maximizing leverage of global, national, multi-regional, regional and local accounts
Develop client strategies, or coach Key Account Managers in the development of their client strategies, and direct, coordinate and/or track their implementation
Drive client prioritization and investment recommendations to focus on opportunities and clients who deliver meaningful business volume, have good growth upside, and yield attractive returns on investment. Conversely, facilitate evaluation, recommendations and decision-making on client accounts and opportunities of lower investment priority
Lead capture strategies for key pursuits and major projects within the regional market and ensure those strategies yield high capture rates
Lead market specific external affairs and branding activities that promote AECOM
Provide analysis and performance forecasts against business plans, and when necessary make timely adjustments of priorities to achieve plans
Ensure the proper staffing of Key Account positions, in coordination with the National Market Sector Director
Provide mentoring and coaching to Key Account Managers
Advanced degree in Environmental related studies
Sales and marketing experience

Pharmaceutical Process Engineering Technician Resume Examples & Samples

Direct activities and support supervision of contracted resources
Perform diagnostics of automation systems
Provide support and troubleshooting on a wide range of process, facility and utility automation systems
Identify and manage high value cost and time savings
Participate in new processes to improve efficiency and cost savings
Participate in continuous improvement program to maintain instrument support within a given budget
Identify problems and inefficiencies in processes and methods, with proposed solutions
Maintain accurate and complete records supporting GxP operations
Read blueprints, P&IDs and technical documents related to operations/facilities
Efficiently use CMMS to request and direct work flows
Prioritize, plan, provide for minor and major repair efforts
Make effective use of PdM, PM and predictive maintenance techniques
Provide data to assist with forecasting budgets, training needs, capital purchases and staffing needs
Maintain a positive, can-do attitude while seeking opportunities for cost savings both inside and outside of the immediate team
Maintain GMP compliance for all assigned work
Develop and follow SOPs on maintenance and repair of process equipment, instrumentation and controls
Assist in the execution of IQ/OQ/PQ protocols
Provide the Customer Relations Manager with recommended work priorities for CMMS generated work requests
Participate in planning sessions with the customer, maintenance manager, planners, schedulers, and technicians
Support system owners in performing reliability assessment, efficiency improvements, and strategic planning
Participate in “Management of Change” process for equipment modifications
Perform corrective action for abnormal events or system failures including issuance of incident reports
Maintain CMMS database for assigned assets and optimize spare and replacement parts inventories and purchase
Order parts and schedule vendor support
Comply with and enforce AECOM and company policies and safety practices, procedures and guidelines such as job hazard analysis, lockout/tagout, and the use of PPE
Operate various measuring, diagnostic and testing tools, instruments and software to perform troubleshooting, work completion and to provide energy efficiency solutions
Maintain a strict schedule in order to be successful in the assignment and meet expected client service levels as established by the Company
Be flexible in the day-to-day activities and shift scheduling for the benefit of the customer’s mission
Comply with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP)
Respond to emergency calls (by phone or in person) during off-hours and determine resources needed to mitigate problem (AECOM or subcontractor)
Perform other duties as assigned by the AECOM Program Manager
Working knowledge of process instrumentation maintenance and/or calibrations
Bachelor’s degree in an Engineering or related technical field
Experience performing maintenance and calibrations on process instrumentation
Experience troubleshooting, programming, or working with DeltaV, Foxboro, Allen Bradley, OSI PI, and/or OPC interface
Experience with direct repair and/or maintenance of automation systems
Understanding of Service Level Agreements (SLA) and Key Performance Indicators (KPI)
Understanding and alignment of recordable metrics to customer needs for Financial Management
Experience with GxP compliance in pharmaceutical environment
Specific knowledge of pharmaceutical manufacturing compression practices and hands on experience in the operation, setup, repair and modification of tablet presses such as Kilian & Korsch
Specific knowledge of pharmaceutical manufacturing encapsulation practices and hands on experience in the operation, setup, repair and modification of capsule filler machines such as Macofar & Bonapace

Inbound Pharmaceutical Customer Care Resume Examples & Samples

Responds to requests and calls from customers related to client specific programs and products
Identifies and responds to customer’s needs based on designated procedures of account/client
Makes attempts to resolve issues and deescalate issues of irate or dissatisfied clients
Tracks call related information of each call received for auditing and reporting purposes
Provides feedback reports on call issues related to downtime and/or training issues
High School Diploma or GED required; graduation from a college with an Associate’s degree preferred
Phone related customer service
Familiarity with Microsoft Windows, Word, and Excel applications
May require client specific bilingual language requirement, as necessary
Knowledge of product/procedures
Ability to stay composed and objective
Patience/empathetic
Mental Acuity
Conversational
Confident/Assertive
Demonstrate a positive attitude

Pharmaceutical Account Manager Resume Examples & Samples

Grow revenues to set targets
Develop customer management strategies
To be the account manager for a number designated accounts acting as the principal contact between the client and RSSL operation teams in order to achieve sales growth
Optimise calls by ‘selling-on’ other services to the client, where appropriate
Monitor multi laboratory projects, ensuring that work is carried out in a timely manner and reports are sent out as per customer requirements
Assist the Customer Services team as required at periods of peak demand to ensure that clients are provided with a professional service and act as the liaison between RSSL lab staff and clients
Generally assist the Head of Sales (Senior Group Leader Sales) and wider commercial team as required
Represent RSSL at external events (conferences, exhibitions, seminars, industry meetings) in order to grow sales
Support the Commercial team with the co-ordination and collation of RFI’s proposals and tenders as required
Know the ethical and legal compliance responsibilities of the position; raise questions and concerns when faced with an ethical or compliance issue; apply integrity in all aspects of professional conduct
Customer service and sales experience
Have a proven scientific background with recognised qualification - HND or equivalent qualification
Have an understanding of laboratory work and its application to solving customer problems
Full UK driving licence
The personality and technical credibility to develop excellent working relationships with both clients and laboratory staff
Outgoing proactive approach, energy, drive, enthusiasm and the ability to motivate others
Team player, plus ability to work on own initiative
Excellent inter-personal skills, with the ability to interact effectively by telephone, written communication and face-to-face
An organised approach, capable of working on several projects at any one time
Experience within the pharmaceutical industry

Pharmaceutical Sales Rep Neurology Floater Resume Examples & Samples

1 + years pharmaceutical sales experience
Product launch experience preferred
Successful completion of all sales training requirements
Ability to perform the duties of a pharmaceutical representatives
80% travel - weekly overnight travel may be expected
Ensure a safe work environment by following all safety and ergonomic rules, including any special personal protective equipment (PPE) and standard operating procedures (SOP's) applying to a particular process or area
Ensure product quality by performing in-process checks, complying with current good manufacturing practices (cGMP’s), being alert for unacceptable quality of incoming and outgoing materials, initiating quality improvements and participating on quality improvement projects
Communicate quality and other problems to supervision in a timely manner
Dispense components, operate, clean, set-up, change and maintain equipment and rooms to manufacture products
Clean and maintain process equipment which may include, but not limited to tanks, filler pumps, blenders, mills, presses, coating pans, etc
Operate electric or manual hand trucks for most stocking operations as well as forklift operation as needed
Accurately record on the appropriate documents, the process / manufacturing steps, production results, equipment in-process checks, samplings, cleanings, ingredients used, and any other relevant information
Maintain daily production sheets and time sheets for team
Take ownership of personal training and learning to develop skills to continuously improve processes
Help build team-oriented culture by motivating and supporting team members by sharing knowledge with all members of the factory to continuously improve the process
Properly dispose of waste product and containers
Inform department administrative assistant when to order supplies as needed
May perform other duties as assigned
At least 6 months experience using motorized and non-motorized material handling equipment
At least 6 months experience using automated inventory system or equivalent computer systems (i.e., SAP, MES, Microsoft Software, etc.)
Must be able to fluently read, write, and speak English
Proven ability to work safely in a production environment
Proficient mathematical skills and familiarity with the metric system
Demonstrated knowledge of Windows and Lotus Notes
Previous experience in a government regulated (i.e., FDA, GMP, etc.) environment
An adaptable, flexible, dependable, team player with strong communication, learning, self-managing and decision-making skills
A proven ability to identify and solve problems, plan and organize and share knowledge
Post high school education

Pharmaceutical Handler EFL Miramar Resume Examples & Samples

Responsible for the let down process to ensure that sufficient quantities of product are in the pick location
Maintain cleanliness and organization of pharmacy storage areas
Advise inventory analyst of out-of-stock or short dated items upon discovery and rotate stock as necessary
Ensure all shipments are labeled correctly
Maintain effective communication with customers, co-workers, and other team members
Maintain all material handling equipment and report any potential problems
Skill in operating a fork lift vehicle
Technical skills – able to operate a fork lift vehicle and a motorized pallet jack
Actively participating in client discussions and meetings
Communicating a broad range of Firm services; and,
Managing workstreams within client engagements, including preparing concise, accurate documents and maintaining project economics while maintaining flexibility for unanticipated issues
Manufacturing / Packaging Operations,
Supply Chain Planning,
Engineering,
Facilities,
Cost Accounting,
Warehousing and logistics,
Distribution and logistics,
Process review, redesign and implementation,
Productivity and efficiency,
Clinical resource management and/or value analysis,
Distribution or distributor assessment, recommendation and optimization,
In-sourcing and/or outsourcing assessment,
Purchase services review and assessment,
Contracting non-labor cost reduction,
Inventory and par management,
Account payable invoice discrepancy management,
Supply chain IT,
Technology assessment and optimization,
GPO assessment, selection and optimization,
Capital asset management, and,
Analysis and communication
Understanding personal and team roles
Contributing to a positive working environment by building solid relationships with team members
Proactively seeking guidance, clarification and feedback
Developing and sustaining client relationships using networking, negotiation and persuasion skills to help to identify and sell potential new service opportunities
Preparing and presenting written and verbal materials including RFPs; and,
Assisting with defining resource requirements, project workflow, budgets, billing, and collection

Pharmaceutical Research Practice Lead Resume Examples & Samples

Ability to travel 50%
Master degree or higher in Biology, Chemistry, Clinical Sciences or a related field
Minimum 15 years combined executive leadership experience in a Life Sciences Research organization and/or Consulting experience. Function head within a Life Sciences Research organization preferrred
Minimum 10 years leadership experience managing teams; proven ability to build, manage and foster a team-oriented environment
Deep understanding in one or more of the following: pharmacology, biologics, genomics, cheminformatics, translational science
Expertise in research / laboratory processes and methods, assay workflows, data management and data curation
Experience in one or more of the following: knowledge mining, scientific data curation, target profiling, drug repositioning
Significant client impact and value creation
Issue-based problem solving
Structured communications
On time and on budget high quality project delivery
Significant experience with research informatics software and solutions, including research platforms, workflow systems, and data aggregtation, management and curations solutions in the Research / Early Discovery spaces
Experience working with executives in Life Sciences R&D, with network of existing clients
Significant responsibility leading teams and exceptional team building/ mentoring skills
Excellent leadership, client-facing communication (written and oral) and interpersonal skills
Follow-on project sales and ability to sell work to new clients
Technically savvy and/or interest in working with technology as part of identifying and delivering solutions to clients
Experience with scientific software/ knowledge management solutions
PMP certification (or equivalent)

Pharmaceutical R&D Regulatory Technology Consulting Manager Resume Examples & Samples

Orchestrating and bringing together expertise from across the entire organization—strategy, consulting, digital, technology and operations—to deliver value to clients
Selling the full breadth of Accenture’s services
4+ years of experience with regulatory information management tools in a consulting, implementation or support capacity, with exposure to all phases of a regulatory information management tool implementation including requirements gathering, development, deployment and support preferred
4+ years of experience managing a team of multiple direct reports, clients and vendors
Typically we work at client sites. Depending on your location and specific project responsibilities, this position may require up to75% travel (Monday – Thursday)
Proven ability to build, manage and foster a team-oriented environment
Desire to work in an information systems environment
Excellent communication (written and oral) and interpersonal skills
Excellent leadership and management skills
Understanding of key Pharmaceutical R&D processes andtechnologies. Familiarity with industry-standards such as ICH, IMPD, XEVMPD, Experience with the software development lifecycle, specifically in a validated environment
Experience owning a defined portion of a project, and a demonstrated ability to manage issues and risks, with an understanding of appropriate and timely escalation
Experience managing client and vendor relationships. The abilityto identify and articulate the value of new business opportunities

Pharmaceutical Research Resume Examples & Samples

Leading the effort to define the team structure, framework and approach on new assignments, managing junior team members, aligning with client expectations and tracking to delivery of high quality, timely work products
Identifying, assessing and solving complex business problems within Research, leveraging in-depth knowledge and industry experience in chemistry, assay data management, OMICS, biologics, translational science, etc
Conducting or overseeing industry and client research and analysis to identify industry trends and opportunities for improvement within Research / Early Discovery and Preclinical
Leading the design, development and implementation of business operating models, including vision and strategy, business processes, organizational and governance structures, supporting tools and templates, and performance metrics
Overseeing change management activities, developing communications, training and job aids to support Research capability implementations
Contributing to the growth of Research / Early Discovery capabilities within the R&D Consulting Practice by leading new business proposals and presentations, participating in recruiting activities, and providing coaching and mentoring to consultants and analysts
Bachelors of Science degree or higher
Ability to travel up to 75% Monday through Thursday
Minimum 5 years combined Life Sciences industry and Consulting experience
Proven experience in managing complex technology implementations in the life sciences and/or data management industries
Experience working with executives in Life Sciences R&D
Proven experience leading teams and exceptional team building/ mentoring skills
Experience working in a top tier consulting firm
Experience with data management and curation within Research / Early Discovery
Experience with business analysis and process design within Research / Early Discovery
Understanding of bioinformatics market / bioinformatics software market
Understanding of research / laboratory processes and methods

Pharmaceutical Analyst / Consultant Resume Examples & Samples

Pharmaceuticals
Biotechnology
Medical/Surgical Devices
Project Delivery: Work on small to medium-size teams to deliver projects for global clients. Responsibilities may include strategy and process design in the following areas

Pharmaceutical Services Delivery Team Leader Resume Examples & Samples

Work in close collaboration with the DC-based program team, service delivery advisors in field offices, and local ministries and NGOs as appropriate to assure effective and efficient program strategic design, work planning, and implementation
Provide strategic technical leadership and expertise to MTaPS technical staff on the implementation of high-quality pharmaceutical service delivery, including prioritizing interventions and adapting best practices to local context
Build on existing tools and develop or adapt approaches to ensure the efficiency, acceptability, and impact of services
With other program staff, review, develop, and prepare project training and communications activities in the area of pharmaceutical service delivery
Remain current with the latest international technical developments in pharmaceutical service delivery, including best practices developed by implementing partners, international organizations, and the private sector
Build and maintain technical support network between program technical teams to ensure strategies and tools are appropriately applied in strategic intervention areas and challenges are shared to achieve program goals and objectives
Represent the program at international and local technical meetings and fora, as deemed appropriate by the program director, related to areas of responsibility, and relay lessons learned to program leadership and appropriate technical staff in field offices
Actively participate in operations research and monitoring and evaluation activities, dynamically seeking out and using available data to inform strategic and implementation decisions
Contribute systematically to program communications activities, including informing relevant international and national organization about project approaches, achievements, and challenges through face-to-face communications; contributing to the development of success stories; drafting, editing, and finalizing regular project reports as required by USAID; contributing to project blogs and other electronic communications; and any other communications activities as requested
Assist in the identification of short term technical assistance needs to support program activities and help to identify local and international consultants as necessary
Foster and demonstrate a workplace inclusive of creating opportunity, serving others, building trust, innovation and exceeding expectations
Perform other duties and responsibilities as required
Advanced degree in pharmacy, public health, health policy, or related field
At least 5-8 years’ project management experience in senior-level positions of large, complex international health sector development programs
Minimum 4 years of experience working in developing countries on pharmaceutical systems strengthening, with specific experience in improving and informing service delivery
Demonstrated outstanding leadership, strategic thinking, organizational, team-building and representational skills
Proven success as a decision-maker and respected supervisor overseeing professional and support staff, especially those in remote locations
Demonstrated experience in capacity-building and in working effectively with local NGOs, governments, and the private sector
Proven ability to function effectively with U.S. Government-funded cooperating agencies and contractors, host-country counterparts and government officials, USAID Mission staff, and representatives from other key stakeholders such as NGOs and other donors
Experience working with USAID, Global Fund, or other donors supplying healthcare commodities highly preferred
Demonstrated leadership, versatility, and integrity
Excellent verbal and written English communication and presentation skills are required; fluency in a second language is highly desirable
Associate Director or Senior Manager in a manufacturing or supply chain function within the life sciences industry, and
Prior consulting roles, including a Manager or Senior Manager at a consulting firm in a supply chain function with prior roles within the pharmaceutical life sciences industry
Financial analysis and modelling,
Operational excellence, including operations strategy development, implementation, and due diligence,
Strategic sourcing,
Supply chain planning,
Clinical supply chain planning,
Inventory management,
Manufacturing footprint optimization,
Identifying and addressing client needs: building, maintaining, and utilizing networks of client relationships and community involvement; communicating value propositions; managing resource requirements, project workflow, budgets, billing and collections; and preparing and/or coordinating complex written and verbal materials
Performing as a team leader: supervising teams to create an atmosphere of trust, leverage diverse views, coach staff, and encourage improvement and innovation

Pharmaceutical Sourcing Manager Resume Examples & Samples

Minimum of 5 years experience in project, event or meeting management, at least 2 of which are in procurement required
CMP designation preferred
Experience in hotel buying required
Proven negotiation skills
Knowledge of domestic hotels and destinations required, international a plus
Knowledge of travel supplier operations, overall capabilities/range of services
Program management system experience preferred, especially with an online sourcing tool
Understanding of and ability to effect win/win solutions
Operations experience in hospitality industry or equivalent a plus
Prior successful experience in developing and maintaining key client and supplier relationships
Prior experience in effectively handle multiple projects/demands
Strong knowledge of program/event management and budget maintenance
Ability to travel by airplane, boat, rail and/or car

Pharm Sci Intern Pharmaceutical Ops & Clinical Supply Resume Examples & Samples

Contribute to research experiments to 1.) Improve and/or enhance the biopharmaceutical performance of the drug product or 2.) To develop the manufacturing process using commonly employed unit processes
Support the GMP manufacturing of clinical supply drug product
Support the installation/qualification of new technology/equipment in the pilot plants
Available for 10-12 week internship beginning June 2017
Strong personal character and ethics
Superior communication and interpersonal skills
Excellent academic achievement and analytical ability
Good team player and ability to work independently
Knowledge of commonly employed pharmaceutical unit operations to manufacture drug products is preferred
Operate and clean the following manufacturing equipment/systems
Minimum GCE ‘O’ level/SPM or NITEC/Higher NITEC/Diploma in Biotechnology/Biomedical/Electrical & Electronics/Mechanical/Mechatronics Engineering or relevant disciplines with 2 - 5 years of manufacturing experience in Pharmaceutical/Petrochemicals/Chemicals/Semiconductor or related industries
Fresh NITEC/Higher NITEC/Diploma graduates are welcome to apply
Good understanding of safe working practices and cGMP
A good team player with positive learning attitude
Must be willing to accept the following work condition

Process Project Manager Pharmaceutical Technology & Support Resume Examples & Samples

Support of direct knowledge transfer between the manufacturing sites, support of development of global key technology platforms, technical expertise and Manufacturing Division technology network
Facilitation of communication and interface for manufacturing sites to other global departments such as SCM, Regulatory Affairs, Pharma R&D, Strategic Procurement and CMO Organization
Support or lead investigation teams established to solve major quality issues occurring with our AH pharma products
Master or PhD degree in Science (Process technology, Pharmaceutical technology, Industrial Chemistry, Food technology,…) and at least 10 years of experience in technology or manufacturing position in a Pharmaceutical, Food manufacturing or Fine chemicals producing company or in extended experience in an academic environment of Pharmaceutical/Chemistry departments
Business Experience in projects as site to site and R&D to site transfers will be asset
Project management skills
Regulatory background incl. FDA and EMEA requirements or motivated to acquire this quickly
Strong knowledge of GMP requirements or motivated to acquire this quickly
Experienced in internal business processes and organization
Travel requirement: willing to travel to the different AH Manufacturing Division production locations (40 % of the time)
Language requirements

Senior Project Manager Pharmaceutical & Biotech Market Lead-sf By Area Resume Examples & Samples

Demonstrated ability to manage small projects to medium projects with a life sciences background
Experience in delivery of projects in an operating facility and coordination with owners various project shareholders
Act as one of the company’s prime contacts with the client and is responsible for overall work progress and technical performance on the program
Program utilizes well established program management procedures
Lead and manages the program team through all phases of program planning, mobilization, execution, and closeout consistent with established program delivery processes to the meet the scope, schedule, budget and other specified requirements stated in the contract
Oversee the delivery of the scope, schedule, and budget commitments are defined in the contract. Criteria of strategic importance to the client are often included in the contract as well, and typically define additional commitments required of CH2M HILL to achieve delivery success (e.g. HSE criteria, quality criteria, critical path milestones)
Complete the scope of work to the satisfaction of the client and key stakeholders, while simultaneously ensuring that CH2M HILL’s HS&E, quality, financial, risk management, business and policy expectations are met
Play a role in the business development activities leading to the award of the contract. This typically includes client relationship development, program-specific positioning activities, teaming arrangements, proposal preparation, orals presentation, and contract negotiation consistent with established business development processes
Bachelor’s degree in applicable discipline or equivalent experience
12 - 20+ years progressively responsible Project Management experience

Lead Process Technologist Pharmaceutical & Biotech Resume Examples & Samples

BS Degree in Chemical or Bio Engineering
Minimum 15 years of experience in the design of both Pharmaceutical and Biopharmaceutical facilities
Must have excellent communication skills in a Business Development (BD) “support” role

Director, Pharmaceutical Benefits Resume Examples & Samples

Present the Pharma vision at client presentations, industry conferences
Meet with clients to review drug plan design and performance
Develop strong relations with the various provincial governments to represent our customers best interests (e.g. contribute to proposed legislation)
Establish SLF as a recognized Pharma leader in the insurance industry
Provide our Business Development team with material and consultation for client presentations
Work closely with the key Pharmaceutical Industry Stakeholders (e.g. Pharmacy, Manufactures, Wholesalers) to find partnering opportunities
Generate innovative / creative ideas that align to our strategic objectives around product and service opportunities in the Pharma space
Accountable for the success of the Pharma service offering
Build and influence effective two-way communication with key business partners, specifically business development, incorporating their view into the strategy
Be an active contributor representing Sun Life on associated industry committees as applicable
Contribute to Sun Life’s understanding of the competitive landscape
National travel is required
Practicing pharmacist is preferable
Business background with an understanding of group benefits environment and product development

Manager, Pharmaceutical Manufacturing Resume Examples & Samples

Plans, schedules, directs, evaluates, and manages the complex day-to-day work of manufacturing associates to meet the department goals in terms of quality, productivity and efficiency under cGMP conditions. Proactively identifies and manages quality and compliance deviations, and ensures that corrective actions are implemented. Responsible for conducting pre-campaign risk assessments for the shift team, and compiling post campaign lessons learned. Modifies plans and procedures to suit business demand based on production results
Coaches and develops complex operations and skilled technical staff through talent and performance management of all direct reports. The manager will also develop and maintain resource planning tools in order to project staffing needs and manage cost for the shift team. The manager will work with internal and external staffing recruiters to manage head count needs for the shift team. Further, the position will be responsible for identifying critical gaps in staff training and establishing a development plan for all direct reports that is in line with the overall department goals
Ensures work environment related to assigned area of manufacturing meets company and industry standards and compliance regulations. Leads the development of compliance and safety goals for direct reports. Reviews any issues related to manufacturing performance, process and safety in order to ensure safety, compliance with regulations and cGMPs. Responsible for driving and facilitating continuous process improvement to meet department needs. Develops and maintains Key Performance Indicators (KPI) in order to monitor health of the shift and drive performance management within shift team. Responsible for investigating, developing and evaluating potential solutions to identified safety issues
Continuously evaluates process performance to identify areas of improvement, and collaborate in developing protocols to achieve same. Evaluates and applies modern operational excellence tools to reduce process variability and steadily deliver measurable efficiency, productivity or quality gains
Collaborates within department and cross-functionally to meet set objectives. Represents Filling and Visual Inspection on cross functional teams and gains alignment on day-to-day manufacturing issues and needs
Leadership experience preferred

Pharmaceutical & Life Science Med Device Manager Resume Examples & Samples

Managing teams through the design and implementation of people, process and technology changes, including building solid and collaborative relationships with team members, fostering a productive teamwork environment, leveraging diverse views to encourage innovation, and helping develop and grow team members throughout the course of every engagement, providing timely and meaningful feedback
Exhibiting capability in thought leadership, development of intellectual property (IP), and marketing and promotion of IP
Supporting incremental business development opportunities, and where possible, identifying new business opportunities, including client lead maturation, proposal development, and close. Leveraging industry contacts to make introductions and connect the firm to potiential clients (short term or long term). Maintaining an active rolodex and pipeline of executives and working to maintain, expand, and mature those over time
Identifying and addressing client needs: build, maintain, and utilize networks of client relationships; manage resource requirements, project workflow and budgets
Communicating complex material effectively in written and oral formats to various audiences
Conducting and directing quantitative and qualitative analyses of large and complex data

Senior Pharmaceutical Claims Specialist Resume Examples & Samples

Administers the receipt, validation, and payment of rebate claims for branded NDCs from insurers, prescription benefit managers (PBMs), and at- risk Medicaid organizations (accounts)
Reads and interprets contract terms and conditions concerning rebate eligibility and set parameters in the proprietary contract system (CARS) to accurately calculate each rebate
Processes each claim in accordance with contract language and internal processing procedures
Understands all systems and processes and strives to identify improvements
Assists manager in training and development of claims administration staff
Reviews and interprets rebate contract terms and conditions and establishes parameters in the contracting system (CARS) to produce accurate rebate calculations
Conducts initial quality check, including formulary compliance, on all claim submissions to ensure rebate eligibility. Resolves issues with account and prepares validation system (ECP) to receive detail claim data
Reviews suspect claim records and determines if record should be disputed for payment. Communicates disputed records to account
Prepares contracting system to receive validated claim data and calculate rebates. Ensures accurate system results by manually checking calculations
Acts as the primary contact point for rebate questions from account, account managers, Contract Administration, and Forecast Administration
Supports the collection and recording of data critical to contract performance assessment and rebate forecasting
Managed care rebate claims processing, compliance, or contracting
Experience with Revitas-CARS, -Validata, -ECP, Model N, RxMax, or inPharmative software systems
Technical reading or contract interpretation
External client support/interaction
Advance MS Excel/Access skills
Pharmaceuticals industry
Manipulation of large data sets
Negotiation/conflict resolution
Able to understand and trouble shoot electronic data processing systems
Able to construct system workarounds in special circumstances

Senior Director Pharmaceutical Manufacturer Relations Resume Examples & Samples

Development and execution of a Pharma manufacturer engagement strategy. Developing and successfully implementing strategies and action plans for establishing and enhancing a competitive contracting approach for Cigna which meets current and future needs of our customers and clients
Build and direct effective strategic relationships, contracting initiatives, and strategies with both brand and generic pharmaceutical manufacturers
Continually explore market to develop new contracting opportunities. Maintain and educate organization on industry trends, risks, and opportunities
Strategically partner with CIGNA Pharmacy Management Clinical Program Management to align contracting options to meet client requirements, coverage criteria and formulary strategy
Lead a team of contracting professionals in their daily work
Strong analytical background, business oriented, strategic thinking capabilities and attention to detail, while maintaining a "big picture" view.” Linking results to business performance drivers, generate alternatives, future options and drive positive change
Highly collaborative individual with ability to influence others and build strong professional relationships, especially in a highly matrixed organization
Understanding of the financial principles and operations of the business and able to drive profitability
A comprehensive understanding of contract negotiations, pricing models, network & strategy, products and claim operations, including reimbursement
Ability to integrate functional unit needs and competencies with those of other functional units in the organization in order to maximize overall service efficiency and response. Possesses a comprehensive understanding of functional areas and the impact on overall performance. Has the ability to see business needs outside of ones own work area and to drive a cross-functional agenda
Excellent written and oral communication skills. Ability to create, execute and communicate a strategic vision
Strong relationship management skills and experience
Independent decision maker and risk taker
Ability to lead, manage and mentor a team
Minimum of a Bachelor’s degree in a Life Sciences discipline; MBA preferred and Pharmacist certification preferred
8-10+ years of professional strategic and leadership role in PBM, Managed care, or pharmaceutical contracting and pricing strategy with a strong, successful track record is required
Financial Acumen and Effectiveness Measurement
Negotiating
Risk Analysis and Selection
Understanding Client/Customer Needs
Strategic Thinking
Project Management
Manages relationships and service delivery for assigned books of business. Serve as a resource and point of escalation for assigned clients and staff. Collaborates with several internal Walgreens departments to ensure client satisfaction is achieved through the best service possible to help drive retention and increase sales. Resolve manufacturer customer issues by working internally with appropriate key operational teams
Manages customer relationship with key strategic pharmaceutical and biotech accounts. Identifies opportunities within existing books of business to increase account penetration and capitalize on contract and procurement opportunities
Supports implementation team for all manufacturer contracts and programs
Provides a collaborative customer-facing, problem-solving environment with Sales, Marketing, Operations, and systems with the vision of enhancing Walgreens market leadership
Develops and fosters positive inter-and intra-departmental working relationships with other departments and business units
Provides monthly status updates to manager
Provides support on special projects as needed
Bachelor’s Degree and at least 2 years of experience in a client management function in the healthcare industry or business to business service industry OR a High School Diploma/GED and at least 6 years of experience in a client management function in the healthcare industry or business to business service industry
Experience communicating both verbally (on phone, one-on-one, to groups) and in writing (emails, letters, reports, presentations) to various audiences (work group, team, company management, prospective acquisitions, external clients)
Experience in diagnosing, isolating, and resolving issues and recommending and implementing strategies to resolve problems
At least 1 year of experience with client negotiations including negotiating contracts, prices, resolving service issues and reconciling differences
Basic level skill in Microsoft Office 2003: Word (creating documents, entering and formatting text, page layouts, creating tables, and adding graphics), Excel (creating worksheets, entering data, creating basic formulas, working with cells and rows) and PowerPoint (creating a new presentation from a design template, adding and removing slides, entering and formatting text, adding speaker notes, and viewing presentations)
Experience presenting to and coordinating senior level meetings, including preparation of agendas, documenting meeting minutes, sending out documents to attendees
Willing to travel up to 30% of the time for business purposes (within state and out of state)
Master’s degree / MBA

Pharmaceutical & Life Sciences Regulatory Affairs Resume Examples & Samples

Coordinating/preparing regulatory submissions (e.g., implementing submission templates, overseeing quality control of regulatory documents and submissions etc.) and product registration packages for local regulatory agencies
Facilitating meetings and otherwise maintaining relevant communication with local regulatory agency staff throughout the product approval process
Establishing timely updates and maintenance of global product listings, facility registrations, licenses, approvals and annual registrations
Investigating regulatory history of similar products to assess approval or registration implications
Collaborating the local teams to identify key regulatory requirements for projects and business initiatives
Assisting with the preparation of routine reports and regulatory agency communications; development, updating and maintenance of paper/electronic regulatory document archival systems; and, reviews of promotional/advertising or educational items
Identifying and addressing clientsâ€™ or managersâ€™ needs, including actively participating in client or management discussions and meetings; preparing concise, accurate project documents; and, communicating with clients in an organized and knowledgeable manner (e.g
Participating in practice development and thought leadership opportunities including, but not limited to client proposal development efforts, assisting with service/solution creation or enhancement, publishing industry whitepaper, and attendance at industry conferences

Pharmaceutical QMS Investigator Resume Examples & Samples

Minimum education BSc. In Biology, chemistry or related fields
Experience: 5 years pharmaceutical testing experience. 5 years experience in root cause investigations
Skilled in pharmaceutical testing individual who has experinece / capability to perform thorough investigations into root cause analysis
Knowledge of OOS Investigation regulatory process
Knowledge and experience of using root cause analysis tools
Thorough knowledge of scientific principles pertaining to records under investigation
Works well under pressure and tight deadlines
Ability to work fast and make timely decisions where required (e.g. hypothesis testing, repeat test approvals e.t.c.)
Proven time management skills. Managing multiple assignments
Deliver results in a timely manner
Proven track of working well with others
Excellent written and verbal communications
Candidates must be proficient in using various type of computer software (Word, Excel, PowerPoint, Outlook etc.) and be able to demonstrate good keyboarding skills
Always be able to adhere to full compliance with the company’s Health & Safety, Code of Integrity, and Professional Conduct policies
Appropriate attitude, constant vigilance attention to details and following training SOP for training and training records
Work collaboratively with cross-functional teams to complete competitive bid and strategic sourcing projects for pharmaceuticals and other related goods
Monitor and report on Humana’s pharmaceutical purchases, pricing, and cost of goods sold and margin metrics
Manage the day-to-day activities associated with Humana’s primary and secondary wholesalers, GPO’s and diabetic product suppliers
Complete supplier contractual pricing audits to ensure contractual pricing adherence
Ensure Humana’s pharmacy distribution locations have access to pedigreed and quality pharmaceuticals from reputable sources of supply
Identify and analyze cost of goods improvement opportunities associated distributors and group purchasing organizations
Perform competitive pricing analyses to ensure Humana’s pharmaceutical pricing is competitive across different wholesale sources of supply
Manage day-to-day supplier relationships with wholesalers, distributors, GPO’s, and diabetic product suppliers
Track and reconcile financial metrics within wholesaler and other category supplier agreements
Develop and implement processes, methodologies and tools to forecast and model financial opportunities and communicate with business owners

Pharmaceutical Clinical Research Specialist Resume Examples & Samples

Bachelor's degree or higher in a Science or Engineering discipline from an accredited institution
Minimum of three (3) years clinical research experience
Experience in one or more of the following areas: clinical study coordination, pharmaceutical development, clinical trial management including contracts, clinical trial project management
Demonstrated experience in computer skills including Microsoft Word and Excel
Good organizational, IT, and administrative skills as the job involves a lot of documentation and recording of information through computerized processes
Ability to work effectively on cross-functional teams

Manager Pharmaceutical Strategic Sourcing Resume Examples & Samples

Bachelors degree in Business Administration or a related degree is required
Minimum of 5 years of experience in a related field
Experience with sourcing ideas and identifying/protecting intellectual property
Superior interpersonal, verbal and written communication skills able to communicate effectively and interact with personnel at all levels of technical ability and expertise
Applies advanced knowledge and understanding of concepts, principles, and technical capabilities to manage a wide variety of projects
Recommends new practices, processes, metrics, or models
Works on or may lead complex projects of large scope
Projects may have significant and long-term impact
Provides solutions which may set precedent
Independently determines method for completion of new projects
Receives guidance on overall project objectives
Acts as a mentor to less experienced colleagues

Pharmaceutical Sourcing Resume Examples & Samples

Generic launch / pipeline management
Business analytical support
Budget and forecast support
Risk and opportunity management & reporting
Daily & weekly reporting
Develop innovative purchasing programs
Identify market opportunities and risks
Ensure adherence to the sourcing program
Support resolution of supplier operational issues
Resolve product supply issues
Coach and develop the team
Create and manage budgets and forecasts

Pharmaceutical Director Resume Examples & Samples

Support the development of innovative purchasing programs
Build and maintain relationships with suppliers
Develop and execute negotiation strategies with 140+ supplier partners

Pharmaceutical Production Supervisor Resume Examples & Samples

Perform Investigations and determine and implement long lasting corrective and preventative actions
Monitor process performance, identify gaps, and implement corrective actions to achieve and sustain agreed upon performance
Foster and maintain a continuous process improvement mentality within the group
Foster and maintain Communication within the group
Be able to coordinate activities with other groups and management
Lead the implementation of CAPA items
Operate assigned equipment and processes, as needed
Review and Approve Batch Records and other Documentation
Create Processes and Procedures
Supervise the technical set up and technical personnel's activities for the Filling, Capping,
Participating in pre-FAT testing for new production equipment. This will require some
Mechanical aptitude is a must
Leadership and communication (verbal and written) skills and ability to be part of team
The clean room manufacturing environment requires personnel with good personal hygiene
Adaptability to change and to perform under pressure with time constraints
Bachelors Degree and a minimum 3-years supervisory experience, preferably in the pharmaceutical industry
Must have aseptic pharmaceutical experience
Experience in a manufacturing environment or advanced mechanical training is a plus

Industry Director Pharmaceutical Segment Resume Examples & Samples

Drive corporate relationships by understanding customer life cycle and contract timeframes
Coordinates needs and opportunity assessments across locations
Measures customer satisfaction and develops strategies to improve
Drives the Request for Proposal process
Identifies target profitability, terms and conditions
Coordinates and communicates business development initiatives and strategies
Creates and manages the account strategy and implementation plan
Conducts business reviews with customer
Provides direction to managers/sales representatives on expectations for the servicing account
Drive market share improvement and identify standard marketing programs/promotions relevant to customer
Evaluate customer performance for contract compliance
Bachelor’s degree; MBA preferred
10+ years of relevant work experience; strong background in science and the specific industry segment
Demonstrated ability to maintain and grow senior level customer relationships across multiple areas like Sourcing, Production, Research, Materials Management
Strong financial analysis, negotiation, and project management skills
Strong leadership skills in a matrix environment
Proven sales record

Area Sales Professional Pharmaceutical Resume Examples & Samples

Identify, qualify and develop new opportunities with current and new customers, based on Siemens Portfolio
Develop and maintain knowledge of competitive products and create sales support materials to promote Siemens products vs. the competition
Provide sales assistance and knowledge of the Siemens technology
Create and deliver presentations to customers during sales visits
Gather and communicate input from field to marketing regarding market trends, customer satisfaction, competition, product issues
Work closely with the Market Development team in executing strategies needed to meet the business objectives
Support local sales management in presenting the technology to potential new customers
Develops and communicates a clear strategy for the area/market and achieves business commitment and support
Position Siemens as a key partner to customers and enables top level strategic discussions
Creation of opportunity “Win strategies”, defining customer spend strategy, competitive environment and identifying business development requirements
Develops and presents technical proposals, including Value Proposals
Guides customers to develop investment plans that are feasible within cost, time, and environment constraints
High availability for travel constantly achieving a high productivity
Discipline and organization to achieve a time balance of 75% in activities with customer and 25% in office activities
Discipline and organization for use above 70 per cent of working time in activities against and for the customer, reaching a high productivity
Abide by all business compliance requirements in line with Company policies
Develops strong personal relationships with the customer and leverages this to achieve better sales and business results
Delivery excellent customer service & monitor customer satisfaction levels
Able to spot previously unidentified business opportunities
Frames and communicates strategic opportunities into the business
Energized by creating better ways of doing things, so that higher levels of sales performance can be achieved
Electrical Engineering Degree
Technical Discipline preferred
Wide knowledegement of the Pharma industry
Wide knowledgement of the service portfolio
Prior experience with electrical equipment
Team building
English language (read, write, speak)

Security Shift Supervisor Pharmaceutical Co-driving Resume Examples & Samples

Communicates staffing needs on shift to Account Manager or Operations Manager
Assures that officers receive appropriate training, developing them in both technical and professional skills; also may
As a condition of continued employment, employee must maintain current active status of all required License at all times,

Business Development Manager, Pharmaceutical Resume Examples & Samples

Develop new business opportunities in the Pharmaceutical market in line with the Avery Dennison Marketing Plan
Develop a solid network of relationships with key decision makers at Pharma companies to build a solid opportunity pipeline and drive the overall adoption of pressure sensitive technologies
Work closely with Pharmaceutical Segment leader to define product and service strategies that drive segment growth and profitability
Develop deep understanding of key packaging trends in the Pharma industry and derive implications for future label stock demand
Provide commercial team and customers with segment related information and strategy through training, meeting, reports
Co-work with other segment BDM’s to leverage general marketing capability of Avery Dennison
Strategy & Implementation: Define market & product plans, which clearly establish product positioning (or product differentiation strategies) versus competitive products, product development direction, service programs, pricing & margins guidelines and profitability targets. This includes the development of new market and/or applications
Growing the Business: Define and drive short and mid-term product plans and longer term product roadmaps and end use customer program. Grow the business by developing and introducing new and up-graded products to address product gaps in the market
Product Launches & Support: Conduct competitive product assessments and develop new product or product positioning strategies to compete. Drive product launches with communication and training. Ensure that new products are introduced professionally, with appropriate positioning, pricing, sales materials, promotions and accompanying services. Seek end user insights to create new ideas/products for specific segment requirements with PLT teams
Relationships: Establish and maintain in close co-operation with LPM Asia Pacific, a successful long term product strategy to achieve required sales value and margins along with the objectives (manage product life cycle)
Product Portfolio & Inventory: Manage the regional product portfolio to ensure that the right inventory and/or products are manufactured or kept at the distribution centers & plants
Measurement and Analysis: Assess current revenue performance and monitor product profitability. Partner with organization (Sales / BDMs) to ensure development of programs, tools initiatives to improve performance. Manage products with respect to forecast, packaging, range, logistic requirements, etc
Margin: Manage product profitability
Participate as a member of the PLT team, share best practices, learning’s and strategies across the regions
Support Sr. Marketing manager to develop new marketing initiatives that contribute Avery Dennison China business

Senior Pharmaceutical Account Manager Resume Examples & Samples

Lead high value opportunities as required
To be the account manager for a number of designated strategic accounts acting as the principal contact between the client and RSSL operation teams in order to achieve sales growth
To lead the development of, and cross sell service offerings to, a number of strategic accounts
Represent RSSL at external events (conferences, exhibitions, seminars, industry meetings)
Provide support to Head of Sales to understand market needs, trends, competitor awareness to influence the commercial strategy and subsequent new service opportunities
To contribute to company strategic initiatives and projects as required
Generally assist in activities leading to the development and growth of the RSSL business
Monitor strategic clients multi laboratory projects, tracking that work is carried out as per customer requirements and ensuring that key dates are met and if issues arise, step in to coordinate client responses
Have a proven scientific background with recognised qualifications – Degree, HND or equivalent qualification
Extensive customer services and sales experience
Extensive experience in a relevant market
Technical credibility with the ability to develop excellent working relationships with both clients and laboratory operations staff
An organised approach, capable of working on several projects at any one time and able to prioritise requests
The ability to offer valuable advice and guidance on a broad range of scientific techniques to clients
The ability to create solutions to complex scientific and business issues
English fluency

Senior Pharmaceutical Application Engineer Resume Examples & Samples

Ph.D. in a science or engineering discipline from an accredited university
Minimum of one (1) year (academic or industry) combined pharmaceutical, biotechnology and/or bioprocessing experience
Ph.D. degree in Biochemical Engineering, Chemical Engineering, or Bioengineering from an accredited university
Strong background in biopharmaceutical processing such as monoclonal antibody, recombinant protein or vaccine expression, purification and/or production as demonstrated through a track record of technical publications
Minimum of two (2) years of pharmaceutical, biotechnology or bioprocessing experience gained in an industrial environment
Demonstrated leadership skills and the ability to influence people and organizations at multiple levels
Strong written and verbal communication
Ability to work independently to complete projects, as well as, work with cross-functional teams
3M Global Terms of Use and Privacy Statement
Leading the preparation of regulatory strategies and regulatory submissions (e.g., implementing submission templates, overseeing quality control of regulatory documents, and creating submissions etc.) and product registration packages for local regulatory agencies
Facilitating and leading meetings and maintaining relevant communication with affiliates and local regulatory agency staff throughout the product approval process
Establishing timely updates and maintenance of global product listings, facility registrations, licenses, approvals, and annual registrations
Collaborating with local teams to identify key regulatory requirements for projects and business initiatives
Overseeing/preparing routine reports and regulatory agency communications
Building, updating, and maintaining paper/electronic regulatory document archival systems
Assisting with promotional/advertising reviews or educational items; and,
Monitoring and reporting of regulatory project timelines
Identifying and addressing clientsâ€™ needs, including actively participating in client or management discussions and meetings, managing engagements or projects effectively (e.g., preparing concise, accurate documents and balancing project economics management with the occurrence of unanticipated issues), and communicating with clients in an organized and knowledgeable manner (e.g
Leading teams through creating a positive environment by monitoring workloads of the team while meeting client or management expectations and respecting the work-life quality of team members, providing candid, meaningful feedback in a timely manner, and keeping leadership informed of progress and issues
Participating in practice development and thought leadership opportunities including, but not limited to client proposal development efforts, service/solution creation or enhancement, industry whitepaper publications, industry conference attendance and/or speaker sessions

Pharmaceutical Scientist w Resume Examples & Samples

Pharm.D with 3+ years experience in the field of professional information analysis in life science industry using advanced analysis technologies using databases and controlled vocabularies/thesauri/ontologies OR
Master degree in biomedical life sciences in Pharmacology, Biology or Medicine with 4+ years of professional information analysis in life science industry using advanced analysis technologies (including text mining) databases and controlled vocabularies/thesauri/ontologies. In addition, 3+ years experience in the field of professional information analysis in life science industry using advanced analysis technologies using databases and controlled vocabularies/thesauri/ontologies
Scientific expertise on molecular targets, diseases, biological compounds, processes and technologies
Detailed knowledge about content, structure, and limitations of pharma related information sources
Good technical grasp, creativity and innovative mindset
High degree of reliability, confidentiality, and ability to work under pressure; flexibility and excellent communication, presentation and organizational skills
Fluent in spoken and written English
Develop, evaluate, and implement business critical retrieval and analysis technologies (text, data mining and visualization) with focus on pharmacology, biomedical, technical and business/competitor information
Development of new and augmentation of existing controlled vocabularies (thesauri) and ontologies reflecting all major areas of activity of global BHC
Identification and evaluate new information sources, databases, applications & techniques for information professionals as well as for BHC professionals, scientists, project leaders and senior management
Analysis of information retrieved from commercial text mining applications for BHC core Development interests and activities
Retrieval and analysis of high quality information from databases, literature and competitors for BHC R&D processes and projects
Provide in-depths analyses, reports, recommendations mandatory for strategic decisions (go/no-go decisions in R&D projects, licensing, etc.) in particular at relevant decision points
Provide information for new BHC applications,litigation cases and for due diligence

Pharmaceutical Marketing Analytics Consultant Resume Examples & Samples

Lead cross-functional teams to implement client solutions w
Leverage and customize proprietary analytics to client needs, resulting in exceptional client value
Manage multiple projects ensuring exceptional client satisfaction and on-time delivery
Make presentations and recommendations to clients on optimal customer, sales and marketing strategies and tactics
Contribute to development of new solutions and analytical models
Manage and mentor a team of analysts

Quality Specialist, Pharmaceutical Resume Examples & Samples

The Contractor Quality Analyst (CQA) provides Quality support to the Incoming Material Supplies Inspection processing and laboratory areas
The CQA, with guidance from the Incoming Materials IPT Quality Leadership Team, will perform activities that support and ensure process quality and data integrity with incoming sampling of raw materials and inspection of primary packing components
The Contractor Quality Analyst will become knowledgeable in Federal and other regulatory agency requirements and cGMPs to assure that all areas in compliance, and will train on and gain competency in activities to support incoming sampling in Classified D and C processing areas and component inspection
Support regulatory audits
Submit Work Orders to maintain compliance within sampling and component facilities
Update Supplies Inspection protocols, logbooks, etc. as needed
Support Capital Project actions to ensure compliance of new facility
Proactively identifies areas of continuous improvement in Supplies Inspection
Actively participates in the Tier process and uses this forum to escalate concerns and best practices
Collaborates with IPT members in the identification and implementation of continuous improvement initiatives and action plans
Bachelor's degree. Technical emphasis in an appropriate scientific or engineering field preferred; candidates with majors in other fields will be considered if accompanied by significant relevant experience
At least one year of relevant post-degree work experience in a laboratory, manufacturing, or quality position
Basic understanding of GMPs and of regulatory requirements as they apply to the pharmaceutical field or a related area
Familiarity with vaccine and/or pharmaceutical processing
Familiarity with the batch release process is a key skill necessary for success in this position; prior batch release experience is a strong plus

Pharmaceutical Regulatory Affairs Consultant Resume Examples & Samples

Assist with the Regulatory Affairs review of Licenses
Oversee the preparation of US regulatory documents
Prepares and updates regulatory documents
Works in conjunction with management for review of quality and soundness, including regulatory action and readiness of regulatory documents
BA/BS degree in life sciences
A minimum of 2 to 4 years consulting with pharmaceutical organizations
Sound knowledge and exposure to the relevant US/international regulatory requirements for drug development
Demonstrated experience with License Review

Pharmaceutical & Medical Products Resume Examples & Samples

Experience and / or strong interest in digital health and analytics
Excellent problem-solving, organizational, and analytical skills
Strong multi-tasking abilities
Strong sense over proactiveness
Professional attitude and service orientation; team player
Strong work ethic and “can do” attitude
Great communication skills with people at all levels
Highly inquisitive and creative individual who is excited about working in a cross-cultural environment
Strong people skills and the ability to coach, motivate and inspire younger colleagues
An undergraduate degree from a respected institution with demonstrated analytical expertise is required
Three plus years of operational experience preferably working in a research or business environment
Solid understanding of economic, financial, and general business concepts and terminology
Strong IT skills, including proficiency with Excel, Word, PowerPoint, and basic business tools

Thailand Future Leaders Programme Pharmaceutical Resume Examples & Samples

Bachelor’s Degree Equivalent (or will graduate within the next 4 months) in Pharmaceutical, Bio Medical Sciences, Business Administration or Sciences. Master’s degree is a plus
No more than 2 years post graduate work experience (if any)
Strong professional skills and good academic results
Authorized to work within Thailand
Analytical skill, drive change, influencing skill and commercial awareness
Location mobility is required and must be able to travel
Fluent in Thai and English (written and spoken)

Esprit Commercial Pharmaceutical Resume Examples & Samples

MBA degree within the past 2 years (2015, 2016) or completion of an MBA degree by spring 2017
At least 3-5 years of commercial work experience prior to business school
3-5 years of commercial work experience
Must be eligible to work in Russia at the time of, and for the duration of employment and be able to furnish evidence of work authorization
Must be willing to relocate domestically and internationally in any one of the 100 countries where we operate
Multiple examples of delivering a significant value to enhance a business
Strategic decision making that positively impacted a project and/or organization
Commercial (Pharmaceutical) experience overseas, and/or experience working in a large multinational corporation or consulting with large matrixed organizations
Desire to develop a career in general management within the healthcare industry
Experience or knowledge of GSK commercial pharmaceutical practices
Applications open 8th September 2016

Pharmaceutical Waste Chemist Resume Examples & Samples

Ensures Health and Safety is the number one goal by following policies, processes, and acting in a safe manner at all times
Collect waste pick-ups throughout customer facility
Conduct chemical bulking/consolidation as required
Proper packaging of waste to maximize efficiency and maintain compliance
Inspect drums for container integrity and regulatory compliance
Safe loading and unloading of waste hauling vehicles
Transporting waste material to a Clean Harbors facility
Assist with all Clean Harbors activities on site as needed

Pharmaceutical QC Chemists Resume Examples & Samples

The QC Chemist shall conduct analytical and physical tests on raw materials, drug substances, in-process samples and drug products in accordance with approved procedures, with minimal supervision of the laboratory supervisor
The incumbent will, on occasion, supervise the work of one or more Technicians, if deemed necessary by the Laboratory Supervisor
The incumbent should be able to demonstrate a working knowledge of all required analytical techniques used in the QC Laboratory
He/she should be able to perform all required duties independently or with minimal assistance of the lab supervisor
The incumbent shall assure that products are tested and evaluated in accordance with laboratory SOPs and cGMP regulations and are dispositioned accordingly
The incumbent should be fully aware of version and change control as they relate to all lab documentation
He/she shall maintain laboratory instrumentation, logbooks, test results, databases and notebooks in compliance with laboratory SOPs and cGMPs as they relate to the QC Laboratory (i.e., 21 CFR 211.65)
The incumbent should be fully aware of all USP/NF and other compendial requirements, ICH and FDA Guidances, Corporate laboratory requirements and other policies and procedures as they relate to QC Laboratory activities
The incumbent will be responsible for providing and documenting training to less experienced laboratory personnel
He/she maintains a safe work environment for self and others in the laboratory. Assures that all safety information such as MSDSs are available for all lab personnel
The incumbent may be called upon to perform other tasks to support the attainment of business objectives
The incumbent is responsible for mentoring less experience lab personnel in good documentation practices (notebook, investigative and other technical report writing, annotating and archiving supporting data, maintaining procedural formats, etc.)
The incumbent may perform such metrology functions as instrument/system calibration and qualifications
Possess at least a Bachelor’s
3-5 years of experience in the pharmaceutical industry
The incumbent must demonstrate excellent verbal, written and interpersonal communications skills
In that there are stringent requirements associated with the pharmaceutical industry a high degree of accuracy, commitment and integrity is required
The incumbent should exhibit proficiency in software such as Microsoft Word and Microsoft Excel
Please submit resume directly to the posting

Pharmaceutical Documentation Specialist Resume Examples & Samples

Writes technical documents such as methods, specifications, validation protocols and reports, transfer protocols and reports based on corporate policies and SOPs, compendial, ICH and FDA regulatory guidance
Ensures that the integrity and accuracy of all laboratory documents are maintained
Assess overall document compliance with protocols, SOPs, company policies, and applicable regulations
Evaluates compendial documents and reviews procedures for analytical development and validation
Reviews Drug Master Files (DMFs) of active ingredients and provides essential information to laboratory personnel
Reviews analytical data for accuracy, completeness and compliance to cGMPs and established laboratory documentation standards
Generates change requests required for analytical documents and routes documents for review and approval. Assigns document numbers. Maintains hard copies and electronic files of technical documents
Communicate with raw material manufacturer for technical information
In a timely manner provide AR&D documents required for CBE, PAS, and ANDA submission to Regulatory Affairs
Manages satellite copies of method specifications and technical documents
Additional tasks or responsibilities as assigned
Scope of Responsibility
Collaborates with colleagues and external partners to achieve primary department goals
Ensures compliance with cGMPs, DEA regulations, and site operating procedures under the direction of management
Works in coordination with project plans and goals as assigned by management
BS or MS in a scientific field with at least five to eight years of experience in the pharmaceutical industry
Excellent computer skills and competence with Microsoft Office Suite (such as Word, Excel, PowerPoint, and/or Access)
Must be able to work independently
Must have an appropriate understanding of ICH and FDA regulatory guidelines to prepare documents properly
Must have an understanding of FDA and DEA regulations
Must be familiar with proper cGMP practices for analytical laboratories and working knowledge of basic laboratory instrumental analysis and wet chemistry skills
Physical Requirements

Pharmaceutical Meeting Manager Resume Examples & Samples

Travel required: 40%
Keep abreast of industry standards and trends related to responsibilities
Develop and maintain key client and supplier relationships
Develop and maintain knowledge of technology and/or software solutions
REQUIRED:5-7 years meeting planning experience with at least 3 years in a pharma environment
CMP preferred
4 year degree preferred
Proven aptitude for technology and/or software solutions and analytical skills required
Microsoft Word and Excel experience – Advanced level
Unique industry offering learning and growth opportunity
Competitive benefits offered day-one on the job
PTO days offered day-one
Tuition assistance plus great training programs day-one
12 hour rotating shifts offer flexibility

Senior Pharmaceutical Administrator Resume Examples & Samples

Work with executive team members, decision makers, and stakeholders to define business requirements and systems goals, and to identify and resolve business systems issues
Insert job responsibility
Collaborate with IT team to ensure smooth and reliable operation of software and systems for fulfilling business objectives and processes
Design and deploy new applications and enhancements to existing applications, software, and operating systems in a Windows Server environment
Perform cost-benefit and return on investment analyses for proposed systems to aid management in making implementation decisions
Field incoming problem tickets from end users to resolve application and software issues within servers, databases, and other mission-critical systems
Perform hands-on fixes at the desktop level, including installing and upgrading software, installing hardware, implementing file backups, and configuring systems and applications
BS in Computer Science, Chemistry or related field
Eight years of relevant IT/support experience. This should include at least five years of Waters Empower (version 1 and/ or 2) support experience as well as five years of computer system validation
Must be very familiar with FDA and GMP regulations as applicable to the pharmaceutical industry, analytical laboratory practices and computer system validation methodologies
Experience with Waters Empower is required. Experience with Electronic Lab Notebook and LIMS is desired
Experience in FDA Pharma environment, 21 CFR part 11, GMP very highly desired
Experience with change management process very highly desired

Pharmaceutical Sciences Systems IT Lead Resume Examples & Samples

Sole contributor or leader of a small team to deliver IT solutions that allow the business to reach its strategic objectives and are implemented in a cost efficient and high quality manner
Has authority and responsibility for a significant area of work, including technical, financial and quality aspects. When appropriate, leads organizational objectives and delegates responsibilities. Is accountable for actions and decisions taken by self and subordinates
Directs business process design and requirements analysis on large/complex project. Ensures documentation according to Takeda QMS standards, policies and procedures
Leads requirements gathering, prioritization and negotiation with business management on a BU level
Is a subject matter expert in the business area of expertise, understands one or more BU organisations and related technical landscapes
Responsible for delivery of large-scale changes and delivery of IT projects
Makes decisions which impact the work of employing organizations, achievement of organizational objectives and financial performance
Influences policy formation on the contribution of own specialism to business objectives. Influences a significant part of own organization. Develops influential relationships with internal and external customers/suppliers/partners at senior management level, including industry leaders
Recommends strategy, validating and justifying business needs, conducting feasibility studies, producing high-level and detailed business models, preparing business cases, overseeing development and implementation of solutions,
Actively shares emerging industry standards/trends with customers and peers within area of responsibility
Assures projects and project team members follow all company and departmental policies, procedures and standards
Ensures delivered solutions are compliant with associated federal regulations (SOX, OFCCP, labor laws, GMP, GxP, GCP, etc)
Proactively identifies and assists in prioritizing opportunities to streamline business and/or system processes
Act as an IT business partner responsible for program planning and project management for the Pharmaceutical Sciences Strategy and Operations area, with a focus on Pharmaceutical Sciences CMC Program Management, Clinical Supply Chain Strategy, and Alliance Management
Lead change management activities and technical assessments of software platforms environments
Lead program area success and system rationalization and alignment with business priorities during periods of transformation and change
Manage selection and support of externalization capabilities for working with Contract Research Organizations (CROs) and Contract Manufacturing Organizations (CMOs)
Lead teams that deliver and maintain FDA 21CFRpart11 compliant solutions to Pharmaceutical Sciences departments in a cost efficient and high quality manner
Interact with vendors and Takeda IT Infrastructure/Architecture to understand system requirements and ensure optimal system architecture for global deployments
Ensure high quality documentation including Configuration and Design documents, Installation and Operational Qualifications, SOPs and execution of validation test scripts
Proactively identify and assist in prioritizing opportunities to streamline business and/or system processes
Bachelors Degree or high school degree and 12 years of work experience in any business related field
8 + years of relevant experience
Extensive experience supporting functional processes and technical design
Extensive experience implementing applications
Excellent user knowledge of relevant systems solutions
Excellent oral and written communications skills, business acumen with problem solving and analytical skills
Ability to write and speak the English language
Bachelor’s degree with 8+ years experience or Masters with 6+ years experience in Engineering/Computer Science/Life Science
5+ years' experience in a scientific or biotech/pharma environment and familiar with drug development processes
5 years+ IT Business Analysis and Project Management experience in a large pharmaceutical environment with validated systems
5 years + experience with deployment of supply chain and pharmaceutical sciences systems
Ability to work collaboratively and comfortable working in a dynamic, cross-functional, and fast-paced global environment
Experience in an FDA regulated environment required
Knowledge of System Development Life Cycle (SDLC) Processes
Knowledge of Clinical Supply Chain and Pharmaceutical Product Development domain
Experience with information systems for lab data including LIMS, and inventory systems a plus
Demonstrated successful management of IT projects, including scope, financial, and schedule goals
Experience working with solutions delivery teams such as corporate IT infrastructure/architecture, applications development & integration, and support
Access to transportation to attend meetings
Ability to fly to meetings regionally and globally
Pharmaceutical industry and/or drug development business experience

Senior Pharmaceutical Process Engineer Resume Examples & Samples

The successful candidate will have design experience of Biotechnology, Small Molecule API Synthesis , Fill Finish, Oral Dosage Facility Design and Operation mainly gained within an engineering design office
Active membership in a professional body, such as the IChemE, ISPE, PDA, EI, etc. is expected as a demonstration of self-development and professional qualification
Ability to work on own initiative and to strict deadlines

Pharmaceutical Process Engineer Resume Examples & Samples

Responsible for performing various process engineering work functions in a manner that will provide a safe and operable plant
Understands obligations and authority to make appropriate design decisions necessary for plant safety and operability
Reviews the unit/plant layout for unsafe piping/equipment arrangement and for adequate access to critical valves
The basic requirement is a chemical engineering degree
The successful candidate will have design experience of Biotechnology, Small Molecule API Synthesis , Fill Finish, Oral Dosage Facility Design and Operation mainly gained within an engineering design offic
Organized and adaptable with a flexible approach to Design experience

Lead Design Pharmaceutical Process Engineer Resume Examples & Samples

Identifies potentially lethal/toxic substances and designs the systems handling those substances in accordance with established Jacobs/Client procedures
Assists in specification of any required safety systems (eye-washers, safety-showers, gas detectors, etc)
The successful candidate will have design experience of Biotechnology, Small Molecule API Synthesis , Fill Finish, Oral Dosage' Facility Design and Operation mainly gained within an engineering design office
Chartered Engineer
Operation of process equipment under strict adherence to cGMP, OSHA and United policies and regulations
Basic trouble-shooting, assist with technical issues
Monitor and audit work processes to ensure compliance and completion of targets
Review and/or execute related documentation
Receive and handle production raw materials
Maintain personal cGMP training to ensure compliance
Work on problems of moderate scope
Identify, develop and implement process improvements
Execute validation protocols for processes and equipment
Ability to navigate sophisticated HMI control systems on automated pharmaceutical manufacturing equipment
Packaging experience preferred
Excellent professional documentation skills, with strong written and verbal communication skills
Team player committed to quality and working effectively
Ability to objectively, accurately, and thoroughly convey complex issues in writing
Ability to interact with other departments effectively
Ability to handle confidential company data, projects, information, etc

Pharmaceutical Pricing Analyst Resume Examples & Samples

Development and maintenance of pharmaceutical pricing and reimbursement benchmarks, indicators and data visualisation based on our proprietary pharmaceutical market access information (pricing trends/levels, market access timelines, reimbursement)
Support for, and delivery, of weekly and monthly editorials, bulletins, analysis and presentations on Pricing and Reimbursement (P&R), including a specific focus on oncology treatments
Maintenance of clinical trial information for reimbursement decisions
Handling large datasets and teasing out trends/analysis
Support for product development on geographic expansion and methodology development
Involvement in ad hoc and consulting projects
Provide support for, and work closely with, the other life sciences teams
Liaising with, and providing support for, sales, editorial and marketing teams to ensure quality products are delivered to clients
Experience in writing pharmaceutical industry based reports; or from a market access background
Background in Excel, data science, VBA/programming
Knowledge of the pharmaceutical and international healthcare landscape
Excellent in written English; extra language a bonus
Problem solver
Works willingly and effectively with others, individually and across the team to accomplish goals
Ability to deliver high quality work with strong attention to detail
Post-graduate degree or equivalent with a preference for health economics, health policy, VBA, statistics, or data science

Key Account Manager Pharmaceutical & Biopharmaceutical Decision Support Tools & Services Resume Examples & Samples

Strategic account development with a focus on managing existing relationships and grow overall revenue by optimizing the client experience and selling new solutions
Conducting knowledge gap analysis for assigned Strategic Accounts
Optimize the customer journey and experience with Decision Resources
Interfacing with all key buying influencers such as direct users of the product, including department heads and global franchise and brand leads
Create, present and execute strategic account and business plans
Expanding the use of their products and services into all appropriate departments within a named account base
Prospecting for new customers and qualifying new leads to support a balanced pipeline for future sales
Generating proposals, planning customer meetings, and demonstrating capabilities on assigned products in a defined territory
Developing and maintaining a high level of product knowledge of their products and services
Business or Scientific Degree preferred
5+ years Sales and Account management experience
Pharmaceutical or healthcare industry experience is a plus
Passionate about winning; focused on energizing client relationships and building relationships at all levels within an organization
Track record of delivering results and exceeding sales quotas
Experience in both territory and strategic account planning
Experience in creating custom proposals and responding to RFPs
Excellent presentation, verbal and written communications skills
Ability to execute on multiple priorities within a fast-paced environment
Clear thinker with proven ability to synthesize complex issues into simple messages
Ability to travel to clients by air, with monthly frequency
Team player, experience of working with cross-functional and international teams
Knowledge of market research or business intelligence
Pharmaceutical processing activities in the DP building and support locations
Documentation of all activities in line with cGMP requirements
Cross training within the team and training of new team members
Participation in continuous improvement programs to implement improvements in
The quality, safety, environmental and production systems
Execution of commissioning and validation protocols on an ongoing basis
A minimum of 1 years experience in Batch processing operations in an FDA/
HPRA regulated industry. A good knowledge of cGMP and regulatory requirements
Relating to the pharmaceutical industry is required
Dangerous chemicals is required
Good I.T. skills are required
The position requires a moderate level of manual work, in the movement, charging
And discharging of raw materials and finished products. All personnel must be able
To accomplish these manual tasks, while wearing appropriate PPE
The position requires a high level of attention to detail and mental concentration, to
Ensure total compliance with manufacturing operating procedures at all times
The position requires proven problem solving skills, and the ability to adapt to new
Manufacturing process on a regular basis
The position requires proven technical skills, to ensure the person can cope with the
Technical demands of the position at all times
Requires innovative thinking, where new and solutions are proposed on a regular basis
Must be results driven striving to meet all targets and metric standards as set by
Site/department and division leaders
Requires total commitment to quality and maintaining a high standard of work at all
Strong communication skills both verbal and written are required for the execution
Of this role
Strong interpersonal skills are required
Understands and Supports the principles of Perfect Performance
Is responsible for the manufacture of pharmaceutical products in line with all
Policies, procedures and regulations
Demonstrates an ethos of Right First Time at all times
Adheres to and follows all procedures policies and guidelines ensuring compliance
With cGMP and HPRA/FDA regulations at all times
The position has a high level of autonomy and individuals are expected to work on
Their own initiative
Shows a high level of tenacity to ensure closure of issues
This position is crucial in maintaining the compliance of validated systems ensuring
That any changes or modifications are documented and actioned
Pharmaceutical manufacturing requires the safe handling of chemicals and potent
Compounds on an ongoing basis
Requires flexibility in relation to meeting the demands of the business through shift
Work and working hours

Pharmaceutical GMP Compliance Associate Resume Examples & Samples

50% - Provides support for Quality Control Systems as needed with primary support for Document and Records Management, Training Program Management, Compliance Management and Quality Event processing (Deviations, Change Controls, CAPAs)
20% - Responsible for the Regulatory Compliance of all functions within their scope
20% - Writes SOPs and Guides supporting Quality Control System processes
10% - Guides less experienced members of the BioCMC group in cGMP interpretation and compliance
5-6 years of experience in the pharma, biotech, medical device or related industry
3-4 years of experience in a Quality Assurance role in a GMP environment
Experience in the implementation and interpretation of Quality Systems supporting analytical testing of pharma/regulated products
Functional knowledge of LIMS and other electronic data systems
Strong knowledge of GMP requirements
Ability to lead Process Improvements
Strong writing skills

Researcher FDA Office of Pharmaceutical Research New Delhi India Office Resume Examples & Samples

Willing to relocate with minimal administrative procedures
Minimum of 5 – 7 years of related experience
Master’s in Public Health or equivalent required
Independent researcher with experience in chemistry particularly analytical chemistry and spectroscopy (At least 2 years)
Strong record of oral and written communication as evidenced by presentations and peer-reviewed publications
Strong leadership qualities and experience working as part of collaborative groups
Experience in data management, processing and analysis
Ability to independently plan, develop and evaluate written plans

Account Manager Pharmaceutical Softgel Resume Examples & Samples

A BS/BA degree is required in a scientific discipline related to pharmaceuticals/biopharmaceuticals
A minimum of 3 years of pharmaceutical contract service sales experience is required
Proven ability to organize and plan work, manage travel, and balance multiple priorities effectively is required
Ability to interact effectively with scientists and technical staff from customers and within the Catalent organization are required
Must be willing and able to travel up to 80% to visit clients as well as meet with clients in Catalent's manufacturing facilities in St. Petersburg, FL (and other international locations as needed)

Pharmaceutical Marketing Resume Examples & Samples

An 11-week intensive, summer program with effective orientation and onboarding program, with an opportunity to work closely with other MBA interns and collaborate with members of Bayer’s Pharmaceutical Marketing and Sales Teams
A practical, hands-on assignment which will have direct involvement in a meaningful mission and allows the chance to demonstrate potential by leading projects or initiatives that will aim to maximize sales, marketing and profit growth for our Specialty Pharmaceutical business
An opportunity to work within a dynamic environment as a key contributor in championing business building ideas and presenting recommendations to Senior Management based on sound business analyses
Competitive salary and housing options
Assessing competitor’s strengths, weaknesses, strategies and plans to recommend options to compete more effectively
Evaluating the attractiveness of specific consumer segments and recommending, as appropriate, how to position brand against these consumer segments
Quantifying incremental sales opportunities via increased distribution in new channels
Evaluating technologies/web based initiatives to increase marketing and sales messages to customers
Determining if consumer promotion programs are driving share of voice, loyalty and/or profitability
Defining internal processes, identify best practices, pain points and opportunities for improvement, as well as, executing projects to disseminate best practices and/or address pain points and opportunities for improvement
Evaluating payer segmentation and recommend options to optimize
Current enrollment in a Master’s of Business Administration program with a minimum of 2 years relevant work experience in Marketing, Sales, General Business (Finance, Supply Chain, etc.) or similar function
Leadership, demonstrated through the ability to lead projects and willingness to work successfully with diverse team members, while establishing and delivering goals in a team or independent work environment
Integrity, supported by a proven record of delivering results by fostering open communication, effectively preparing written communication and speaking/presenting openly and honestly
Flexibility, evidenced in the ability to partner effectively and achieve results through influencing team members and agency partners, while understanding and incorporating customer needs in the decision making process
Efficiency, exhibited through strong financial and analytical skills with the ability to make recommendations based on in-depth quantitative analyses, sound problem-solving and decision-making skills with demonstrated ability to identify key issues, consider customer needs, make well-support fact- based recommendations, and identify and implement appropriate actions within specific deadlines
Previous experience in the Healthcare industry

Pharmaceutical R&D Management Consulting Senior Manager Resume Examples & Samples

Providing strong R&D functional knowledge and expertise to team members
Providing solutions to complex business problems within an area of responsibility, where analysis of situations and/ or data requires in-depth R&D industry knowledge and an understanding of an organization’s objectives
Leading teams (managers, consultants, analysts) on client engagements, with accountability for (1) correct focus and alignment to client expectations, (2) on-time completion of the work, and (3) a work product meeting or exceeding the highest quality standards
Using research and professional experience to develop innovative thought leadership and points of view and to contribute relevant industry insights to project teams and clients
Leading teams in the design, development and implementation of business operating models, (e.g., vision and strategy, business processes, organizational and governance structures, supporting tools and templates, performance metrics), and the related change management activities associated with implementation
Defining the strategic direction of a project team aligned to client interests and expectations, working with the team manager to communicate and execute that strategic direction effectively within the project team
Interacting with senior management at a client and/ or within Accenture, which may involve negotiating or influencing on matters of significant importance
Using latitude in decision making and judgment to determine solutions to day-to-day and project challenges
Managing large teams and/ or work efforts (if in an individual contributor role) at a client or within Accenture
Contributing to the growth of the R&D Consulting Practice by identifying and pursuing new business opportunities, leading proposals, presentations, recruiting activities, and by coaching and mentoring managers, consultants, analysts
Ability to meet travel requirements
7 + years of consulting experience with an emphasis in management consulting
7 + years of experience working in the Life Sciences industry
Bachelor’s degree; science or engineering degree preferred
4+ years working in Life Sciences R&D industry (e.g., clinical development, pharmacovigilance, regulatory, medical affairs), or related areas (e.g., CROs)
Evidence of strategic consulting experience, including but not limited to

Pharmaceutical R&D Regulatory Technology Manager Resume Examples & Samples

Building and sustaining long-term client relationships
Selling and delivering an expanded range of management and technology consulting services
Assess and improve regulatory affairs and regulatory operations processes and their underlying technology platforms
Provide regulatory information management subject matter expertise in areas such as document management, requirements management, submission planning and tracking, submission publishing, and registration and commitment tracking
Typical projects consist of definition of a regulatory IT roadmap, assessment of current regulatory technology footprint and/ or design and implementation of regulatory systems to achieve a desired future state
Other projects may involve the design, development and implementation of regulatory operating models, including vision and strategy, business processes, organizational and governance structures, supporting tools and templates, and performance metrics, along with change management to support these efforts
4+ years of regulatory consulting experience in an IT/systems development environment
Ability to meet travel requirements: depending on your location and specific project responsibilities, this position may require up to 75% travel (Monday – Thursday)
Proven ability to work creatively and analytically in a problem-solving environment
Understanding of key Pharmaceutical R&D processes and technologies. Familiarity with industry-standards such as ICH, IMPD, XEVMPD. Experience with the software development lifecycle, specifically in a validated environment
Prior supervisory and people development experience

Pharmaceutical Manufacturing Supervisor Resume Examples & Samples

Preferred 1 to 2 year’s experience in a pharmaceutical or medical device manufacturing operations, engineering, logistics or quality
Preferred to have some experience in Lean manufacturing principles and / or going through the Black Belt certification process
Ability to anticipate the next processing steps in each manufacturing suite and allocate the appropriate people resources to ensure the production schedule is met
Ability to take current production output standards and determine who/what is preventing from meeting the goal, taking appropriate corrective action, and/or holding those responsible accountable for the misses
Strong leadership skills including being able to provide day to day direction, deliver performance reviews and formal disciplines
Must possess strong written and verbal communication skills
Subject matter expert on their shift for their areas of responsibility
Ability to deliver immediate performance feedback to machine operators operating in assigned areas
Ability to communicate and interact with on-site customers, or their representatives
Perform advanced math calculations
Must work in a safe manner
Capable of making decisions based on both historical data and that achieved through thorough analysis
Must demonstrate working computer knowledge
Direct Reports: 10 - 30
Total Site Staff (includes directs): Technicians, Room Leaders and Sr. Technicians
Handling of raw materials for product assembly
Lifting boxes and/or containers up to 40 lbs. (27.2 kg) from waist to chest height
Overhead lift and reach (≤15 lbs.)
Handling of finished product
Manipulation of drums to and from 6-inch pallets (up to 80 lbs. of force)
Operating in various postures
Overhead reach, squatting, kneeling, and forward bending
Coordination in a laboratory setting, e.g., climbing up/down ladders or maneuvering around drums or between equipment
Operating safely in a dynamic environment which includes mobile and fixed equipment and changing conditions while completing job tasks that range from simple to complex and/or multi-tasking
Accountable for schedule conformance
Allocates people resources on a daily basis to meet the production plan
Enforces disciplinary action for performance, attendance, and etc
Serves as a safety role model, consistently demonstrating safe work habits, and identifying unsafe conditions
Ensures team members wear all appropriate safety equipment and follow all safety procedures
Ensures all required daily safety inspections are completed and turned-in
Ensures their rooms operates under cGMP conditions (swabs, clean status, dress code)
Ensures all related SOPs and batch record instructions are followed at all times
Resolves operational issues on shift, which may include frequent communication with Quality, Supply Chain, Maintenance, and technical resources
May assist with reviewing and confirming batch record correctness prior to submission to QA
Provides immediate feedback to Room Leader and technicians on performance
Participates in the investigation of EIF, deviation, and development of root cause analysis
Attends, and actively participates in, the shift change meeting
Ensures clear communication between shifts
Drives improvement related to applicable Catalent Winchester goals and objectives
Responsible for working with the functional Manager to staff required overtime
Serves as a resource regarding general training issues (e.g. answer questions, assist employees, etc.)
Perform required employee performance appraisals

Intern Pharmaceutical Technology Resume Examples & Samples

You will support us in developing application technology data and new applications for our pharmaceutical excipients
You will also translate the results into technical product information for our customers
You will actively work to find innovative forms of administration and formulations
In addition, you will take on projects of your own in the area of pharmaceutical technology and attend guided tours and workshops
The issue you work on during your internship may be suitable for writing a thesis
You are a student of pharmacy or pharmaceutical engineering and specialize in the area of pharmaceutical technology
Alongside excellent academic records, you have a pronounced interest in manufacturing and application of pharmaceutical excipients
You communicate confidently in English and German as well as you are a proficient user of the standard computer applications
You also enjoy contributing creatively to a team in order to achieve the best results together
An innovative working style and high engagement complete your profile

Pharmaceutical Expert Continuous Manufacturing Resume Examples & Samples

Actively participates in project teams and networks as responsible to development formulations, processes, equipment, and control strategies for continuous manufacturing of solid dosage forms
Actively supports the manufacturing of drug product for clinical supplies under full GMP using continuous manufacturing processes including documentation preparation and review, scientific support and handling of deviations and changes
Identifies options for enhancement of continuous manufacturing capabilities and screening of the continuous manufacturing landscape within the pharmaceutical industry
Ensures quality, quantity and timelines in all assigned projects, networks and/or platforms and coaches associates on target dates and priorities
Evaluates data, interprets results, , draws relevant conclusions, writes reports and actively drives any required implementation
Generates and selects most appropriate scientific documents that are handed over to internal and/or external partners, such as Technical Operations, authorities, or other companies
Proactively supports the generation of international registration documents and interacts with authorities where appropriate
Proactively participates in budget forecasts, prepares and tracks invoices and ensures cost awareness in all assigned projects and/or networks
Interacts and collaborates with other functions in Development to facilitate the transfer of knowledge of continuous manufacturing for drug products
Actively supports the continuous manufacturing unit as a technical expert on audits and inspections
Min. three years of successfully demonstrated directly related experience in drug product development or manufacturing process development in pharmaceutical industry
Proven track record in the development of innovative solutions for drug product manufacturing, e.g. equipment design, formulation or control strategies (PAT)
Thorough knowledge of state-of-art instrumentation/equipment for solid oral dosage manufacturing, preferable in continuous manufacturing
Thorough understanding of development processes in pharmaceutical industry; advanced experiences in continuous manufacturing is desirable
Profound literature search skills
Ability to work in and/or lead interdisciplinary and/or cross-cultural teams
Strong knowledge of relevant regulatory and GxP guidance’s for drug product development and manufacturing. Knowledge of guidance’s related to continuous manufacturing specifically is an advantage
Strong communication, presentation and scientific/technical writing skills
Advanced coaching skills

Pharmaceutical Construction Project Manager Resume Examples & Samples

Familiar with corporate level office construction, laboratories, pharmaceutical construction projects and site work
Familiarity with all construction trades including MEP/FP
Experienced with brownfield and renovation
Able to be proactive in forecasting execution issues
Diligence to see assigned activities to their end by consulting or changing status-quo
10+ years of similar work experience or 5 years of experience with applicable education/degree
Engineering Knowledge: Advanced ability to conceptualize and apply engineering & science principles to specific design or construction issues
Pharmaceutical cGMP awareness – Good ability to understand and implement cGMP as applied to equipment/facilities design and related project documentation
Computer Skills: Proficient ability to use MS Outlook, Word, Excel, PowerPoint and MS Project
Project Management Skills: Fair ability to execute and control/monitor project management processes for assigned activities as directed

Event Manager, Pharmaceutical Events Resume Examples & Samples

As this role is for a Pharmaceutical client candidates will have a good understanding and knowledge of pharma compliance and the regulations that this industry is governed by
Effectively Plan and Manage client projects and deliver outstanding service to the clients specification including research, event proposals, budgets, policies, negotiation and management of suppliers, web registration tools, site visits, and onsite management
Communicate confidently amongst peers to share best practice and with internal and external suppliers
Act as ‘lead agency’ and work closely with all vendors to ensure the best outcome to end client
Venue sourcing for meetings outside of a centralized meetings and events program
Achieve targeted financial results whilst delivering high quality events and demonstrate significant savings on client meeting spend. Financial management throughout the life cycle of an event
Planning, coordination, and execution of group air travel including any applicable transfers
Use resource efficiently and maximize productivity by utilizing the relevant technology. Build basic web registration site with support of a web expert
Undertake continuous self-development and training
Able to work on own initiative and frequently in isolation away from office space
Aware of VAT regulations applicable in all markets American Express and Client process and policy compliance
Strong experience in event or meeting management, with a focus on events associated with global clinical trials
Understanding of the clinical trial process and key stakeholders including end client, CRO, site staff and all associated vendors
Proven negotiation skills and an understanding of the ability to effect win/win solutions
Good knowledge of domestic and international venues and destinations
Experience in maintaining key client and hotel and destination supplier relationships
Knowledge of program/event management and budget maintenance
Meeting Event Management technology system experience preferred with an online sourcing tool i.e. Starcite or Cvent
Operates manufacturing equipment and collects and/or evaluates process data as per written procedures, including product sampling during the manufacturing process
Assists in the troubleshooting and maintenance of manufacturing equipment, including grinder, granulators, scales, blenders, positive pumps, vacuum pumps, dust collectors, among othersProvides support to the mechanic in the reparation and maintenance of equipment according to specifications
Follows lock-out, tag-out procedures before intervening with equipment
Assembles and disassembles mechanical equipment to execute cleaning tasks and process, as required
Performs the cleaning and housekeeping of equipment, utensils, tools and areas, major and minor cleaning, according to establish procedures and documenting in the corresponding sheets. Uses correct identification as per procedures
Supports and/or participates in mechanic reparation and preventive maintenance, ensuring compliance with manufacturer specifications
Inspects manufacturing tools and utensils, maintaining them in good condition and maintaining related documentation
Performs the accountability of materials, ingredients and components in the different stages of the manufacturing process Completes documentation accordingly, following good documentation practices, cGMPs and SOPs. Returns materials and allocates waste in the respective designated areas
Weights ingredients to be used in the manufacturing of product, including activities related to active ingredients like sieving, subdivision and intermediate formulation
Complies with standard operating procedures, batch records, production records, sheets, checklist and process related documentation
Supports in other quality related activities such as product evaluation, statistical sampling, microbiological sampling using aseptic techniques, and others as required
Alerts and informs the supervisor and group leader about any incident that could represent a risk or hazard for anyone or for the manufacturing process. Notifies immediately any accident or safety/environmental incident to the supervisor
Supplies materials to the manufacturing area as needed
Complies with all the training required to perform the tasks, including SOPs, forms, guidelines, Safety and Environmental training
Provides support in the auditing of the manufacturing batch records and related documentation
Keeps the areas cleaned and organized, including using the correct identification according to areas cleaning status. Removes material and product between batches according to procedures to avoid mix-ups or contamination Alerts the supervisor about any potential safety hazard or contamination risk
Participates in continuous improvement initiatives related, but not limited, to cost reduction, process optimization, quality level improvement, output increase
Performs material transactions on the inventory system
Follows site general procedures and policies. Uses the personal protective equipment (PPE) required for the process or task to be performed. Uses the PPE in the right way, according to SOPs, Safety guidelines and training, maintains the PPE in good conditions
Collaborates in investigations on process deviations for the manufacturing area and provides support in the implementation of corrective and preventive actions (CAPAs)
Informs Health Services about any medical condition that could impact the performance of, others and/or the product being manufactured
Complies with environmental guidelines, SOPs, training, guidelines, practices, permit’s conditions, event internal notifications as required, monitors’ process parameters to ensure that weight, temperature, pressure, humidity, or others are within limits and in accordance to requirements established in SOPs and lot documentation. Informs any deviation or potential deviation to the supervisor Takes action as per procedures to avoid or minimize impact to the process or operations
Segregates waste (dangerous, non-dangerous) according to procedures and guidelines. Performs environmental inspections to the waste area as required
Evaluates process data and performs product sampling and inspections as part of the manufacturing process and quality monitoring
Documents manufacturing and cleaning steps as per SOPs, batch records and batch official forms, including inspection, sampling and process monitoring
Assists technical personnel in equipment and process validation, including performing the required sampling according to approved instructions
Documents shift events and status in logs, as needed
Performs other related tasks as required
Technical, associate or bachelor’s degree from an accredited institute is preferred

Pharmaceutical Operators Resume Examples & Samples

Operate filling and packaging production unit for FDA and EPA regulated and less regulated pharmaceutical products
Organize and perform equipment set-ups for production processes
Perform unit and equipment cleaning procedures
Conduct IPC’s at defined intervals
Take samples for QC Lab testing
Record information throughout the process into the batch record and/or log books to ensure compliance
Follow proper trouble shooting procedures when malfunctions occur
Follow GMP’s and SOP’s and plant safety guidelines
Prior GMP experience required
Must be able to work any shift (1st, 2nd, or 3rd)
Talking/listening to others to convey/understand information effectively
Ability to read, understand and execute operating instructions, guidelines, SOPs, and batch records
Prior working experience with FDA, EP & EU regulated products required
Good math skills: adding, subtracting, multiplication, percentages, conversions
Demonstrate ability to work in teams and lead by example
Excellent hand-eye coordination
High level attention to detail
Silver Level WorkKey Assessment required or an Associates or higher degree in lieu of the WorkKey Assessment
Ability to operate equipment in accordance with established safety guidelines and operating parameters
Ability to palletize shippers based on pallet configuration drawings

Scientist Within Pharmaceutical Development Biologicals Early Stage Resume Examples & Samples

For the advanced analysis of proteins and their modifications you develop LC-MS methods
You author/review compiled analytical results and provide comprehensive result presentations to project teams
Regarding stakeholders and interfaces (e. g. project teams, line management) you ensure excellent communication, interaction and collaboration
You consult on analytical strategies for samples originating from upstream, downstream and formulation development
Project Management of Pharmaceutical projects through all project phases: planning; preconstruction, construction, commissioning & validation
Cost Forecasting and financial reporting on projects assigned
Management of Change Orders and procurement process
Project Management with high levels of customer satisfaction
Manage projects to completion on-time, within budget and within the scope of work
Manage Client Project Management Information System (PMIS), including monthly updates of project data
Produce reports and briefings using Microsoft Word, Excel and PowerPoint
Bachelor of Science Degree in Engineering, Architecture, Construction Management or Quantity Surveying
Project Management experience in manufacturing or research & development process and/or building projects
3 to 5 years Cost Management experience in Healthcare/Pharmaceutical process and/or Healthcare/Pharmaceutical building projects
Proficient in Microsoft Word, Excel, PowerPoint, and Outlook
Experience of PMIS systems used to manage capital projects program
Pharmaceutical Facilities/Engineering experience to include office, R&D laboratories, mechanical / electrical infrastructure, central plant, site work, building expansions, BAS, and process controls
Experience in Pharmaceutical building projects ranging up to $10 million in value
Certified as PMP, PE, RA or CCM

Buyer Pharmaceutical Resume Examples & Samples

Maintain and verify drug inventory controls are at a level to meet customer demand. Participate in drug inventories. Assist the call center management with customer issues and communications when drugs are out of stock
Up to 2 years of relevant work experience
Proficient in MS Excel and Word
Strong math skills
Demonstrated ability to meet multiple deadlines and manage heavy workload
ABOUT THE DEPARTMENT Procurement is responsible for purchasing all goods and services through approved channels. Procurement responsibilities include providing information, guidelines and collaboration to facilitate the procurement process. Policies and procedures are continuously reviewed and revised to ensure our company remains efficient and competitive

Janssen R&D Pharmaceutical Development & Manufacturing Sciences R&D Summer Intern Resume Examples & Samples

Candidates must be enrolled in an accredited college throughout the duration of the internship. Completion of a minimum of two years towards a BS or pursuing a MS or PhD in Chemical or Biochemical Engineering; Chemistry/Analytical Chemistry; Biology; Biochemistry; Molecular Biology; Biotechnology; Microbiology; Supply Chain Management or related science or engineering disciplines is required
Previous co-op or internship experience is preferred
Student must be available from May - August and have the ability to work full-time during that time
Extensive PC based skills, including Microsoft Excel, Word, Project and PowerPoint, SAP are preferred (SAP for Supply Chain Management only). Minimum 3.2 GPA is preferred. Local travel may be required
Students must be able to provide their own transportation to/from their work location

Senior Scientist, Pharmaceutical Development Resume Examples & Samples

Responsible for designing and managing formulation development projects leading to clinical evaluation of drug delivery systems for HIV prevention and contraceptive products
Interact with contract labs to maintain scientific quality and timeline management
Responsible for writing and editing portions of regulatory documents including Quality
(CMC) sections of INDs, IDEs, and annual reports
Assist in the development of new concept papers, grant proposals and other funding initiatives
Responsible for preparing written and oral presentations and reports to enable dissemination of project plans and results to stakeholders and the greater scientific community
Assist with specific drug development activities (e.g., animal pharmacokinetic studies, and IND- enabling toxicology studies) as needed
Facilitate project management discussions and participate in drug development meetings
Manage project timelines for assigned projects and assist others in creating project timelines within the product development group
Experience in a relevant drug development/drug delivery environment ideally in the pharmaceutical/biotech industry or equivalent is desired

Director, Pharmaceutical Development Resume Examples & Samples

Position located in Northern VA**
Supervise and lead Pharmaceutical Development staff
Conceptualize and lead development of new drug delivery systems
Coordinate with Preclinical, CMC/Quality and Clinical teams with respect to product development
Influence the scientific and strategic direction of CONRAD’s product development program
Develop, author and monitor project work plans and timelines
Prepare and present technical and programmatic communications to stakeholders
Identify new collaborators and partners to support existing and new product development projects
Request, review and negotiate contract proposals and Oversee/monitor sub awards
Oversee the development, review and approval of technical protocols and reports
Share responsibility for the preparation of chemistry, manufacturing and controls (CMC) and nonclinical sections of INDs, IDEs, and annual reports to the FDA
Develop and write concept papers and grant proposals to support fundraising and expand the product development program at CONRAD
Negotiate arrangements with commercial manufacturers and others
Contribute to, and Interface with legal counsel, on business and intellectual property matters
Contribute to IP protection (i.e., write patent applications)
Interact with other agencies and NGOs developing products on behalf of CONRAD
Experience overseeing pharmaceutical development at both preclinical and clinical development stages
Experience overseeing projects with contract research/manufacturing organizations
Excellent communication and interpersonal skills, strong problem-solving skills, detail oriented
Knowledge of cGLP, GMP, ISO and ICH guidelines
Direct experience with microbicides/contraceptive products preferred; experience with combination drug-device products is preferred
Must be willing to travel up to 25%

Pharmaceutical Equipment Calibration & Qualification Coordinator Resume Examples & Samples

Bachelor of Science degree in Chemistry and or in Biological Sciences or equivalent in experience or training
Minimum of 5 years previous laboratory equipment control experience or laboratory experience with strong understanding of laboratory equipment calibration/PM and qualification’s regulatory requirements
Good understanding of the laboratory quality control processes
Comfortable with sophisticated LIMS IT System
ASQ Certification as a Calibration technician is an asset
Ability ttroubleshoot or diagnose equipment problems as needed to minimize down time alternatively ask Subject Matter Expert
Candidates must be proficient in using various types of computer software (Word, Excel. PowerPoint & Outlook)
Proven ability to manage and coordinate multiple projects in a fast-paced, highly professional environment
Ability to work well with others & independently
Proven time management skills and a strong attention to detail
Ability to interpret and analyze data
Must be highly organized and able to work effectively and efficiently in a demanding environment with frequently changing priorities
Work well under pressure
Extended hours and shift work may be required from time to time
Ensures full compliance with the company’s Health & Safety, Code of Integrity, and Professional Conduct policies
Appropriate attitude, constant vigilance, attention to detail and following Training SOP for training and training records

Sterile Packaging Consultant Tyvek® Medical & Pharmaceutical Protection Europe Resume Examples & Samples

Create Demand through networking with the key stakeholders at indirect customer and specifier level of the Medical Device Manufacturing (MDM) Industry and the Pharmaceutical Industry (Packaging Eng., Regulatory Experts, Quality Managers, Operation Managers, Marketing and to less degree Purchasing and Sales) as well as Contract Manufacturers dedicated to those industries
Support and expand our relationships at Key MDMs
Communicate the value propositions through F2F engagements, lectures, training workshops and digital channels in cooperation with Marketing
Provide to MDM technical and regulatory input and arrange meetings or calls with the internal experts of the team
Promote actively new product launches and identify first usersGather market intelligence information and listen to the voice of the customer. Be the key detector of the MPP team for market trends in WE/EMEA. Share actively learnings with the global team providing input and guidance on business and market strategies
Identify and support new packaging opportunities and defend business at risk. Gather quantifiable information as to size, timing and probability as well as about the specific value chain and product specifications. Use the foreseen software tools for collecting, processing, tracking and presenting such information
Establish professional relationships with the sales and marketing staff of direct customers (SPM) and work closely with them on strategies that facilitate Tyvek® use at key MDMs. Help bridge the gap between MDM/DuPont/ SPM
Managing contact strategies for sales, marketing, technical, application development and leadership
Organize conferences and professional events in cooperation with industry partners
Support market research activities, open doors for customer interviews, administrate VOC and Promoter feedback to enforce continuous product and service improvements
Represent DuPont at Tradeshows, review and develop sales tools
Responsible for the customer data base accuracy, work on continuous improvements of the related software tools
Strong Technical and/or Regulatory background in the Medical or Pharmaceutical Industry ideally related to Packaging or Product protection. A Bachelor Degree is required
Ideally several years of experience in the Medical or Pharmaceutical Industry or the related value chain
Being at ease when dealing with people. Showing strong talent to negotiate, to influence and to listen carefully. Ability to communicate internally and externally with impact
Excellence in being self-driven and organized
Team Player capabilities within an international (global) team
Willingness to travel 40-50%
Language: English required, either German or French at high proficiency level, Italian or Spanish would be an asset

Pharmaceutical Technology Intern Resume Examples & Samples

Exhibit excellent mechanical aptitude
Demonstrate good interpersonal, communication, and presentation skills
Sucessfully handle multiple projects to achieve company objectives
Exhibit competency in use of common computer software packages
Demonstrate ability to work within a project plan
Must have a four-year degree in chemistry, chemical engineering, pharmacy, or related discipline
Must be eligible to work in the US
Students pursuing master or Ph.D. degree preferred
Degree focus on pharmaceutical technology relating to oral dosage forms preferred

Pharmaceutical Development Scientist Resume Examples & Samples

PhD or MsC in pharmaceutical technology, pharmaceutics preferably
10 years or more of experience in product formulation development, especially small molecules (solid dosage form is a must have. Liquid formulation experience is desirable)
Experience interacting with CDOs and CMOs
Ability to communicate clearly in a group setting

Security Officer Pharmaceutical Resume Examples & Samples

Positive attitude and professional appearance at all times
Strong communication skills (both written and oral)
3 years senior executive/personal chauffeur experience, extensive knowledge of the Boston area is a must
Must be able to comfortably drive in all weather conditions
Strict client confidentiality a must
Responsible for the safe and efficient transport of Executive’s in passenger SUV’s, shuttles or vans
Operating vehicle in a safe and lawful manner, while observing all traffic regulations
Operating vehicle in a courteous manner, recognizing that the route traveled in heavily
O Valid MA driver's license with a clean driving record is also a must

Viral Safety Specialist Pharmaceutical Operations Resume Examples & Samples

A master degree in life sciences and specialized in virology
Work experience of at least 3 years in an industrial environment, preferable in pharmaceutical industry
Demonstrable experience with analytical testing of biopharmaceutical products, preferable molecular testing
Demonstrable experience with GMP or other quality system regulations
Accurate, quality- and service-minded
Teamplayer, independent, flexible and a pro-active attitude
Outstanding command of the English language (in writing and speaking). Preference for Dutch speaking skills
Willingness to travel on a regular base internationally (15%)
Based in the Netherlands

Quality Assurance Chemical / Pharmaceutical Resume Examples & Samples

Quality Assurance responsibilities include but are not limited to cGMP documentation review related to product release, facilities and equipment, material controls, laboratory controls, packaging and labeling, and production & process controls
Establish and report metrics related products and processes as deemed necessary by the RQM
Ensure the site manufactures products to meet the requirements of 21 CFR 212 (CGMP)
Responsible for the quality of documentation (control, retention, and archival) to support CGMP activities
Engage and collaboration with operations department to drive quality system and CGMP requirements
Responsible for product release activities per CGMP requirements
Responsible for reporting quality system issues to the regional RQM. This includes timely escalation of discrepancies upon identification
Must be able to work day shift 8 - 5pm Monday - Thursday
Bachelor's of Science degree preferred - Microbiology degree highly preferred
New graduates considered
Effective written and verbal English communication skills required
0-2 years’ experience in a regulated environment, medical device experience preferred
Pharmaceutical or medical device experience a plus
ISO experience a plus
Quality Assurance background preferred
Lifting: Frequent lifting between 55 lbs
Ability to manage several tasks at the same time; Ability to focus on tasks ; Ability to evaluate operating conditions ; Ability to exercise sound judgment Personal Protective Equipment
Ability to see fine particulate and differentiate colors in liquid solutions
Ability to hear, write (English), and speak (English) clearly in order to communicate in manufacturing setting

Pharmaceutical Clinical Research Associate Resume Examples & Samples

Bachelor's degree or higher in a science or engineering discipline from an accredited institution
Experience working in a hospital or clinical setting
Knowledge of Good Clinical Practice (GCP), International Conference on Harmonisation (ICH), and Food and Drug Administration (FDA) guidelines
Excellent ability to multi-task and prioritize
Experience as time served Process Engineer
Experience of working in a pharmaceutical environment
Experience with regulated environment documentation practices
Must be able to lead cross-functional teams in problem solving, development of improvement plans and root cause-analysis
Experience of commissioning and maintenance of complex plant and equipment
Able to read and understand engineering drawings
IT literate (MS Outlook, MS Word, MS Excel,)
Degree qualified engineer or equivalent knowledge and experience
Experience of Improvement Projects (lean, Six sigma)
Conversant in GE Systems (EMS, G&O’s, E-learning, Concern Reporting)

Entry Level Pharmaceutical Sales Rep West Resume Examples & Samples

Pre-call plan to meet health care professionals' (HCP) needs. Leverage data and customer knowledge to build discussions around HCP's and patients’ needs. Deliver accurate and timely follow-up discussions with HCP’s and office staff. Foster ongoing trust with HCPs. Use the Customer Selling Model, to influence the HCP decision making process
Analyze territory information to optimize routing and achieve sales results. Monitor local market conditions for changes that impact business
Utilize sales tools, resources and supporting analysis to plan activity. Develop and execute plans to maximize selling resources
Report and monitor sample and literature use, and maintain accurate records
Distribute product samples in accordance with approved sampling guidelines and marketing literature to physicians and other healthcare providers (HCP’s)
Collaborate with partners on routing and resource utilization to maximize overall footprint performance
Provide feedback to District Managers on market place trends, challenges, programs, response to promotion, and product access. Collaborate with DM to establish goals and implement plans to enhance current skill sets and sales results
Attend all company-sponsored sales and medical meetings as directed by company management
Perform Company business in accordance with all regulations, Company policy and procedures. Demonstrate high ethical and professional standards at all times
Additional duties may be assigned
Meet the production schedules outlined by team and/or Supervision
Assist with technical troubleshooting and preventive maintenance tasks as needed and trained
Take action to safely reduce equipment setup and changeover times
Initiate and establish equipment operating parameters to maximize production, while meeting all product specifications
Ensure product quality by performing in-process checks, complying with cGMPs, being alert for unacceptable quality of incoming and outgoing materials, initiating quality improvements, and participating on quality improvement projects
Communicate quality and other non-compliance issues to supervision in a timely manner
Complete, maintain, and update production documentation (both electronic and paper) to perform material movements, material take-outs and yield determinations by following SOPs and utilizing systems as required such as Systems/Applications/Products (SAP), Manufacturing Execution Systems (MES), Electronic Batch Records (EBRs), etc
Operate motorized and non-motorized material handling equipment for assigned stocking operations as well as stand up and sit down fork trucks as needed
At least 6 months experience using motorized & non-motorized material handling equipment
At least 6 months experience using automated inventory system is required or equivalent computer systems (i.e., SAP, MES, Microsoft Software, etc.)
Good written and verbal communication skills in English
Demonstrated ability to work safely in a production environment
Demonstrated ability to read/interpret/follow instructions in regard to workplace documentation, such as SOP’s, Operator Manuals, Work Instructions, etc
Good PC Skills, including use of e-mail, attaching documents to e-mail required. Previous experience using electronic databases and on-line tools required (i.e., but not limited to, Lotus Notes database, Employee Self-Services on-line tools, automated inventory tracking system, etc.)
Must be willing to work overtime as required, based on production demands
Experience working in a Good Manufacturing Practices (GMP) or standard operating procedures (SOP) environment required. Manufacturing experience

Senior Pharmaceutical Equipment Engineer Resume Examples & Samples

Actively participate in teams, projects, networks and/or platforms
Fulfill all related tasks and responsibilities related to own discipline
Proactively communicate key issues and any other critical topics in a timely manner to the appropriate management level and/or to any other relevant project team member(s)
Design, plan, perform and monitor all assigned activities
Drive and implement innovations in the area of Pharmaceutical Equipment-Engineering at the interface to innovative Process Engineering Engineering
Ensure quality, quantity and timelines in all assigned projects, networks and/or platforms. Support and assign associates in specific projects and/or networks. Coach on target dates and priorities. Proactively contribute to budget forecast, grant preparation and tracking of invoices
Ensure costs and cost awareness in all assigned projects, networks and/or platforms
Optimize scientific/technical related activities in assigned projects, networks and/or platforms
Create and implement optimized processes and procedures for activities within the own area of responsibilities
Actively contribute to engineering related innovations / improvement of tools and equipment in lab and pilot plant. Lead risk analyses and/or peer review and process challenge meetings
Generate and select most appropriate scientific documents to hand over to internal and/or external partners (TechOps, authorities, other companies)
Design, plan, perform/supervise, monitor and contribute to projects related to complex scientific/technical engineering activities and design, plan and supervise scientific experiments
Create and implement efficient and robust engineering solutions and procedures/processes for the design, manufacture and/or analysis of Equipment Prototypes and final Equipment designs
Coordinate with team members and external partners assigned to multiple or complex engineering development activities
Drive appropriate planning of workload and resources internally and externally, controlling costs and timescale of projects or respective project tasks
Evaluate and implement new engineering technologies
Address complex research issues within own discipline and lead and supervise new engineering development activities
Report and present scientific/technical work at internal/external meetings/conferences including patents. Provide technical leadership skill in all activities related to the development of the assigned engineering projects
Industrial experience preferably 10+ years
Successfully demonstrated several years (mini-mum of 3 years) of directly related experience (within relevant industrial setting)

Lab Specialist Pharmaceutical Process Development Resume Examples & Samples

Meet quality, quantity and timelines in all assigned projects
Plan, organize, perform and document scientific experiments/plant activities in collaboration with experienced team members if necessary. Seeks proactively for support and coaching from Project Leader, Scientific Expert or other team members during the whole process if necessary
Plan and perform scientific experiment/plant activities (e.g. physical material characterization, capsule filling process development) and plan, perform and contribute to project related scientific/technical activities under minimal guidance from more experienced team members under guidance. (e.g. contribute to interpretation and report results)
Actively contribute to engineering related innovations / improvement of tools and equipment in lab and pilot plant (incl. CAD drawings)
Provide efficient and robust processes for the manufacture and/or specialized facilities e.g. containment labs as an expert w/ adequate guidance. 6. Provide raw data documentation, evaluation and results interpretation. Propose and provide input for the design of next experiments
Optimize existing methods (lab or plant) and develop more efficient ones
Generate lab procedures, reports and/or instructions and/or SOP’s
Actively transfer procedures/instructions to pilot plant or production, including troubleshooting, process steering controls etc
Communicate and address problems, perform safety and literature searches under moderate guidance from more experienced team member
Keep record of and manage chemicals, intermediates, excipients and solvents within own area of responsibility
Collaborate with other team members to facilitate deliveries of DS and/or DP
Utilize special tools/equipments and/or specialized facilities e.g., containment/sterile labs
Evaluate new lab equipment
Contribute to maintenance of infrastructure/equipment
Actively participate in project teams/meetings/networks
Actively contributes to team goals
Ensure all own activities are aligned with overall drug development process
Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISEC & Novartis Guidelines
Minimum of 3 successful years of experience in industrial setting as associate scientist (promotional pathway) or 3-5 years (for BS) or 1-3 years (for MS)
Awareness/proven experience for safe handling of chemicals, potentially dangerous materials and equipment
Proven scientific and technical knowledge and experience (in industrial setting) in the area of capsule filling (preferably with dosator-, tamping pin- and drum- filling technology)
Good mechanical understanding / proven track record in innovating/improving equipment setup (lab / pilot plant) (experience in CAD models pre-ferred)
Adequate knowledge in scientific/technical areas of collaboration
Proficient with laboratory and/or technical tools
Adequate knowledge of software and computer tools
Actively participate in teams, projects, networks and/or platforms. Fulfill all related tasks and responsibilities related to own discipline. Design, plan, perform and monitor all assigned activities. (e.g. physical material characterization, capsule filling process development)
Drive innovations in the area of Pharmaceutical Process-Engineering at the interface to innovative Equipment Engineering (e.g. active input on the engineering of lab- and pilot plant tools and equipment)
Ensure quality, quantity and timelines in all assigned projects, networks and/or platforms. Support and assign associates in specific projects and/or networks. Coach on target dates and priorities
Proactively contribute to budget forecast, grant preparation and tracking of invoices. Ensure costs and cost awareness in all assigned projects, networks and/or platforms. Interpret results, evaluate data, draw relevant conclusions and write reports
Optimize scientific/technical related activities in assigned projects, networks and/or platforms. Create and implement optimized processes and procedures for activities within the own area of responsibilities
Actively contribute to engineering related innovations / improvement of tools and equipment in lab and pilot plant)Lead risk analyses and/or peer review and process challenge meetings
Generate and select most appropriate scientific documents to hand over to internal and/or external partners (TechOps, authorities, other companies). Ensure quality of international registration documents
Interact with authorities where appropriate. Interact/collaborate with Research and/or other functions in Development to facilitate transfer of knowledge and deliveries of DS and DP
Initiate and lead new scientific/development programs. Evaluate and implement new scientific technologies
Provide scientific/technical leadership for efficient and robust processes for the manufacture and/or analysis of intermediates, drug substances and drug products as per own discipline
Report and present scientific/technical work at internal/external meetings/ conferences including patents. Assume scientific/technical key function in teams, projects, networks, platforms and/or department activities. Oversee maintenance of infrastructure/equipment and required investments

Pharmaceutical Services Inspector Resume Examples & Samples

Participates in the provision of training programs for internal staff, professionals and organizations providing pharmacy and medication administration services
Consults with other division staff and provides information on drug related to develop policies and collaborate on innovative approaches for delivering pharmaceutical products in a safe manner that ensures the health and safety of patients
Knowledge of public health or medical care administration
3-5 years working in a healthcare facility preferably skilled nursing homes and hospitals in an administrative or management capacity
Knowledge of state and federal regulations related to long term care, hospitals, clinics, hospices, home health agencies, rehabilitation facilities and ambulatory surgical centers
Is a licensed health care professional e.g., Social Worker, Nursing home Administrator, etc
Experience consulting with long-term care or skilled nursing facilities
Knowledge of Conditions of Participation, 42 CFR Part 482 for Hospitals and state licensure requirements under 105 CMR 130.000
Knowledge of the principles and practices of clinical and pharmaceutical services within health care facilities
Knowledge of principles and practices of biology, toxicology, clinical chemistry, biochemistry and physiology
Knowledge of standard methods and techniques followed in the administration of medication
Knowledge of the standard methods and techniques followed in medical laboratory tests
Knowledge of the types and characteristics of drugs used in providing nursing care
Ability to understand, apply and explain the laws, rules, and regulations, policies, procedures, specifications, standards and guidelines
Ability to understand the laws, rules, regulations, concerning hospital licensure and accreditation
Knowledge of the methods of general report writing
Ability to gather information through observing and questioning individuals and by examining records and documents
Ability to read and understand documents such as doctors’ orders, medication records, and treatment plans
Ability to analyze and determine the applicability of medical data, to draw conclusions, and make appropriate recommendations
Minimum 3+ years of successful industry experience in the development of pharmaceutical formulations (ideally oral dosage forms, solid understanding of QbD and biopharmaceutics)
Excellent knowledge of laboratory and/or technical tools (in industrial setting) in the area of capsule filling (preferably with dosator-, tamping pin- and drum- filling technology) and broader scientific as well as strategic background
Proficient in utilization of special tools/equipment, lab automation tools and specialized tools
Deep understanding on physical material properties, their adequate characterization and impact of material properties on pharmaceutical process performance
Strong understanding at the interface between Drug Substance and Drug Product
Good knowledge of software and computer tools. Profound literature search skills. Ability to work in and/or lead teams. Strong leadership skills. Strong knowledge of relevant SOP, GLP, GMP. Very good communication skills

Pharmaceutical CMC Manager Resume Examples & Samples

Works with R&D team to establish studies needed to support CMC
Provides review, interpretation and reporting of study data needed to support CMC
Actively participates in issuing protocols, generating and evaluating data, and producing reports to support CMC
Interprets study data
Acts as a technical resource in generating information in support of CMC
Collaborates with Regulatory Affairs to establish plan(s) for building CMC sections
BS in Chemistry, Engineering, or related science
10 years experience in chemistry-related field
Demonstrated experience in project management or PMP Certification
Excellent organizational skills and attention to detail
Deep understanding of FDA-regulated practices

Healthcare / Pharmaceutical PM Resume Examples & Samples

Leads project initiation and planning activities to structure the project, including facilitating the definition of project goals, objectives, and scope. Also engages project teams in detailed planning activities, manages project execution activities, and ensures completion of project closure activities
Coordinates the identification and planning of all project work streams, including working with each functional manager to plan work product schedules, identify key milestones, manage dependencies, identify risks, track and manage issues, and report on project progress
Leads and oversees the identification, execution, and updating of project timelines, tasks/responsibilities, and deliverables
Works with project team to identify project risks, resolve issues, and eliminate project challenges
Monitors and reports on the progress of project milestones and deliverables
Communicates clear, concise, and accurate project status to all appropriate project stakeholders, including providing periodic status reports
Monitors and reports on project progress against planned project data
Coordinates and responds to project changes, including escalating project issues and decisions as needed
Demonstrated familiarity with structured project management methodologies
Proven ability to manage multiple complex projects in various stages of the project life cycle from initiation through completion
Ability to contribute consistently and positively in a dynamic, high-paced, and sometimes unpredictable work environment
Proven ability to facilitate project alignment between business and technical teams
Possesses strong leadership capabilities to lead and direct project teams, including proven ability to build successful and effective project teams, leading team decision-making processes, and fostering an environment of healthy team debate and collaboration
Ability to manage large projects with aggressive timelines and challenging scope, including being able to create and execute project work plans to meet changing requirements resulting from evolving business needs
Analytical problem-solver
Self-directed and detail-oriented
Highly effective organization and planning skills
Excellent written and verbal communication skills, including effective presentation skills
Develops and maintains constructive and cooperative working relationships
Ability to facilitate conflict resolution
Proficiency in project management tools such as Microsoft Project and SharePoint (or similar PPM tool)
Proficiency in using Microsoft Office products (Word, Excel, PowerPoint, Visio)
Knowledge of application development and testing processes (preferred)
Knowledge of business process improvements and controls (preferred)
5-10 years of experience in project management or project leadership role
Project Management Professional (PMP) certification (preferred)

Pharmaceutical Recruiter Resume Examples & Samples

Requisition Management/Pipeline Management
Participate in weekly calls with hiring managers and account teams to discuss candidate and requisition status and health
‘Sell' candidates to hiring managers based on passive recruiting and/or phone interview results
Develop Sourcing Strategies as needed
Internet research and job board posting; develop a strategy to determine which job postings should be on which job boards to develop sufficient pipeline
Accurately forecasts and requests transitional hours in a timely manner, as well as leverages resources to maximize productivity and pipeline management
Report generation and metric analysis
Presentation development and delivery
Utilize and leverage client ATS and ADP RPO ATS to drive performance
Process consultation, design, implementation and improvement

Pharmaceutical Business Development Manager Resume Examples & Samples

Working with global sales channels to grow market opportunities
Delivering market strategy, understanding future market needs and developing and communicating product roadmaps to inform major business investment decisions
Lead product marketing campaigns and promotion, presenting at international conferences, seminars and workshops
Training and supporting the international sales force with joint sales visits conveying both market and instrument expertise
Support the marketing department in production of literature, including brochures, presentations, posters and notes
Interface with the customer community and key industry stakeholders in close collaboration with the sales function
Experience in an international sales or application support role
Practical experimental skills using Raman or other spectroscopic instrumentation
Experience in dealing with sales channels, customers and distributors
Experience of presenting to and training a variety of different sized audiences

Pharmaceutical Construction Manager Resume Examples & Samples

8-12 years of related experience with 5 years of experience at site manager level
BS/MS in Construction Management or Architectural / Engineering Discipline is preferred. Relevant experience will be considered in lieu of a formal degree
Experience with LEAN Project Delivery
Completion of OSHA 30 hour training program is desirable
The successful CM candidate must have recent and broad experience in the design and construction of biopharmaceutical, food and heavy process industry facilities. Types of work should include site development, infrastructure and utility installation (clean and plant), main process areas, finishing and packaging and support facilities to include labs and office buildings
Experience with project $50mm and greater
Ability to travel US Domestic to take follow project to the field

Director, Pharmaceutical Manufacturing Resume Examples & Samples

Provides department leadership and direction for organizing, developing and executing the manufacturing plan; including establishment, execution and reporting of departmental systems, goals, priorities, schedules, risk analysis, packaging capacities, budgets, metrics and timelines
Ensures that the products are packaged in a timely and safe manner which meet or exceed all specifications, quality standards, FDA regulations and other Health Authority guidelines
Defines and recommends key objectives in the manufacturing (Dispensing, Compounding, and Cleaning) area of operation. Develops specific short-term and long-term plans and programs, together with supporting budget requests and justification. Ensures the Department’s performance conforms to operating plans, forecasts, budgets, standards and objectives
Develops and/or reviews protocols, quality reports, events, investigations, customer complaints, cost variance reports, production yields reports and manpower and facilities utilization reports. Formulates and tracks action plans to address issues, opportunities and associated CAPA
Develops, reviews and manages department capital and expense budgets. Rationalizes budget against changes in production forecasts
Partners with Quality, Engineering and Production Management to identify and prioritize the continuous improvement of the dispensing, compounding, and cleaning processes and technologies to improve the quality, safety, reliability, RFT and productivity of the manufacturing and testing processes. Identifies, supports and insures the use of ‘best practices’ and development of new technologies and/or product/process innovations in conjunction with Quality, Engineering, Manufacturing and Process Development
Selects, develops and maintains qualified personnel in all positions, assists in departmental hiring, career planning, succession planning, conducts performance reviews and recommends compensation
Communicates regularly with employees and management about company/department plans, issues, new initiatives and progress against goals. Ensures communication among all Production shifts is adequate to maintain and efficient and quality operation
Identifies and ensures the development of adequate training curriculum for staff, ensures that appropriate training program is successfully maintained and that ‘standard work’ practices are employed
Minimum of a Bachelor's degree (or equivalent) and 5 years of related experience, 10 years related experience preferred. A Master's degree and 5 years of relevant experience desirable. However, a combination of experience and/or education will be taken into consideration
Must possess knowledge of the FDA review process concerning accepted manufacturing policies and procedures, sound administrative management skills, strong teamwork orientation and effective communication skill sets
Proven ability to recruit, train, and motivate personnel in order to balance staffing strength with profitability and growth
Must possess strong analytical, numerical, and reasoning abilities. Strong interpersonal skills and the confidence to lead, direct and motivate a diverse manufacturing staff as a functional leader, while also demonstrating consistency, reliability and effective utilization of teams
May be required to stand, walk, stoop; bend; kneel; and climb step. May require the use of hands and arms to lift and scoop
May be required to wear personal protective equipment including but not limited to: respiratory protection, safety glasses, hearing protection, safety shoes and protective clothing

Pharmaceutical Project Manager FDE Resume Examples & Samples

Seek opportunities to capture and share learning cross-functionally
Identify and bring forth areas for continual process improvement to team and function; identify methods to decrease drug development cycle times and cost
Participate in retrospective project/process review meetings (i.e. after action reviews) to identify issues and strengths and help capture learning
Liaise with Project Management Office (PMO) and with the Resource Modeling and Forecasting Team to identify, share, and incorporate best practices into future iterations of processes, tools, training, or guidance
Pharm. D/Master’s degree OR Bachelor's degree preferably in a health-related, scientific or engineering field with a minimum of 3 years of work experience in the pharmaceutical industry, drug development, and/or project management
Previous experience with or knowledge of drug development processes
Higher degrees or certifications (e.g. MS., MBA, Masters in Project Management or PMP)
Critical chain project management certification or experience with application of critical chain project management principles
Applied knowledge of project management tools and processes (e.g. management of integration, scope, time, cost, quality, human resources, communications, risk, procurement, and stakeholders as defined by Project Management Body of Knowledge)
Strong computer skills; skilled at using Word, Excel, PowerPoint, Microsoft Project and capable of maintaining the appropriate project documentation in SAP
Practical experience performing project management for a cross-functional project

Security Account Manager Pharmaceutical Resume Examples & Samples

Manage a team of security officers, site and/or shift supervisors including hiring/selection, scheduling, payroll, training, coaching, development and support
Ensure the Client Site is provided with high quality security services to protect people and property
Coordinate necessary support services to effectively manage client site to meet or exceed financial and operational goals and provide quality customer service
Assure regular communication of issues or program with Client
Handle any escalated security issues or emergency situations appropriately
Other management responsibilities as determined by Client or District Manager
Develop / maintain operational procedures so that a valid, site-specific OPM and post orders are always available for emergency reference by the security staff
Previous Contract Security, facilities management, military or law enforcement experience
At least 2 years of business management/operations/supervisory experience (depending on size/scope of client)
Ability to develop and grow customer relationships
Experience in hiring, developing, motivating and retaining quality staff
Ability to work in a team-oriented management environment with the ability to work independently
Previous payroll, billing and scheduling experience preferred
Ability to work in a team-oriented management environment while having an entrepreneurial attitude
Key Competencies: Staff Management, Financial Management, Integrity, Problem Solving, Conflict Management, Time Management, Customer Focus, Timely Decision Making, Motivating and Directing Others, Drive for Results
Identify, assess and drive enabling technologies and device innovations to benefit AbbVie’s pipeline and life cycle management of marketed products
With key stakeholders, drive streamlined processes (including design control) for the development of Device/Drug combination products
Partner, communicate and liaise with Product Strategy Teams and organizations to align project specific Combination Product/Device strategies
Lead development of delivery device technology strategy for subcutaneous delivery of biologics
Collaborate with AbbVie’s Commercial organization to develop the business case for investment in device technology platforms
Identify, assess, and develop strategies for enhancing technologies for product ecosystems
Lead and develop a group of engineers and scientists engaged in Combination Product development. Drive creation of processes for technology landscaping and partner selection
Serve on joint Development and Steering Committees for partnered projects

Pharmaceutical Logistics Resume Examples & Samples

Visual inspection of vialled products for pharmaceutical use; work is carried out under GMP
Carrying out visual inspection of filled vials, both freeze dried and liquid filled, using approved procedures
Remove defective products based on agreed reject categories
Reporting of each inspection in batch manufacturing records in accordance with GMP
Sampling raw materials and finished product
Product storage duties
Control of finished product storage and storage areas
Document storage locations per batch in inventory
Ensure storage areas are monitored and perform checks as directed by supervisor
Product labelling and dispatch
Communication with clients regarding labelling, dispatch, stock control etc
Generation of product labels as per client instructions
Labelling of product vials per agreed batch manufacturing instructions
Arranging dispatch of materials to Client/Clinic sites as appropriate
Book transportation to coincide with the size of dispatch to meet the clients delivery deadlines
Review of dispatch temperature traces
Participation in training sessions in support of the above activities
Ensuring training record folders are suitably maintained with appropriate documentation to show competency for each activity performed
Participate in maintaining housekeeping standards and audit readiness of facility
Completion of batch manufacturing records, worksheets, forms and logbooks to the required standard in support of the above activities
Preparation of relevant documentation to support department activities
Communicate and help resolve any customer complaints as necessary
Manage old and damaged product
Participation in customer and regulatory audits/inspections as required
Participation in validation exercises
Leak testing
All other reasonable activities in support of department functions under the direction of the Logistics Supervisor or Production Managers

Pharmaceutical Section Editor Resume Examples & Samples

PharmD degree required
3+ years pharmaceutical experience outside of retail industry
Strong ability to multitask and work in a fast paced environment
Flexible and adaptable, able to adjust to emerging product requirements
Excellent critical thinking and organizational skills
Must be able to evaluate literature and summarize findings
Must be a self-motivator and work independently and as part of a team
Ability to use knowledge as pharmacist to organize and develop drug information based on clinical needs of physician readers
Ability to prepare additional material or rewrite content, as needed and match publication style and requirements
Ability to create new drug monographs (tables) when new molecular entities approved by the FDA and enter them in database
Ability to update database with new indications, new dosage regimens, and other pertinent information (eg, precautions, warnings)
Ability to verify accuracy of content in existing monographs
Ability to identify, correct, and review drug interactions
Detailed oriented, precise, and rigorous regarding the implementation of style guides
Working knowledge of Microsoft Office Suite particularly with Excel and Word

Pharmaceutical Communications Summer Intern Resume Examples & Samples

Develop clear event and strategic communications plans
Evaluate the value of effective corporate communications, both internally and externally
Learn how to navigate a complex organization and manage internal stakeholders
Currently enrolled in a 4-year bachelor undergraduate (minimum) program and pursuing a degree in Communications or related field
Excellent written and verbal communication skills; detail-oriented
Self-starter who can work on multiple priorities in a fast paced environment
Ability to work both collaboratively and independently
Ability to interact professionally with internal stakeholders at various organizational levels
Basic problem solving skills and project management abilities; resourceful
Strong computer skills with Microsoft Office proficiency (Word, Excel and PowerPoint)
Event planning experience a plus

Validation Pharmaceutical Technology Scientist Resume Examples & Samples

Manage/perform site projects focused on Process Validation, process optimization, process trouble shooting and new product introduction
Liaise with site project teams
Evaluate project budgets, forecast, expenditures and accomplishment of objectives and ensure all projects are executed on time and within budget
Open and close change controls for each project as necessary
Review and approve ECR/ECO’s
Assess the effectiveness of current projects and identify possibilities for new projects and opportunities
Coordinates resources from Engineering, Quality Assurance, and production personnel assigned to specific projects
Furnish direction to engineers and technicians regarding project requirements
Develops and communicates project timelines and status
Generation and execution of protocols for both new and marketed products including the qualification of new chemical raw materials and components
Work with other departments to ensure identified work items are addressed in a timely and satisfactory manner
Perform filing, computer input/output tasks and prepare identified reports as required
Address internal and external customer queries under the guidance of the department supervisor/manager
Assure our business practices enhance the welfare of our customers, employees and community in which we operate
Ensure that all activities are fully compliant with all criteria established by governmental agencies, Ministries of Health and legislative requirements
Maintain a clean and organized work area
Assist Allergan in achieving environmental, health, and safety goals by working safely and observing all general plant and department safety policies
Perform all assigned duties according to departmental SOP’s and cGMP’s, and company policies
Remain current on proper procedures by reviewing current, revised, and new SOP’s relating to the job and to the department
Complete and remain current with all required cGMP and safety training
Project Management skills and principles
Strong financial and cost accounting skills desired
Knowledge and understanding of current Good Manufacturing Practices (cGMP)
Knowledge and understanding of Regulatory Compliance criteria established by Governmental Agencies, Boards of Health and Legislative Requirements, such as FDA, OSHA, EPA, and DEA
Basic knowledge of strategic and tactical issues in an operations environment
Detail-oriented and self-motivated
Ability to handle multiple projects, duties, and assignments
Ability to read, comprehend, write, and communicate effectively in English
Ability to carry out detailed written or oral instructions
Ability to work and communicate with others in a professional and effective manner, within a team-oriented environment
Knowledge and understanding of personal computer operations, including Windows-based computer systems such as Microsoft Office applications (Word, Access, Excel, PowerPoint, MS Project), with an ability to learn other computer based systems
Understanding of equipment qualification / calibration concepts
Understanding of pharmaceutical raw material tests and raw material characterization
Ability to perform intermediate statistical computations (Cp, Cpk, regression, analysis), and practical application of statistical software
Knowledge and application of process improvement for all types of products
Knowledge of process / cleaning validation processes
Ability to employ sound leadership skills for providing guidance to project teams
Ability to solve practical problems, considering a variety of concrete variables in situations where only limited standardization exists

Senior Pharmaceutical Technology Scientist Resume Examples & Samples

Responsible for the development and pre-validation of analytical methods using multiple analytical techniques including HPLC, CBPA, qPCR, Western blots, UV and other general methods as needed. Develops protocols and SOPs, trains staff and maintains the laboratory consistent with departmental and Allergan requirements. Applies routine and specialized analytical techniques to characterize and quantify biopharmaceuticals. Transfers methods to other manufacturing sites as needed
Assures that select agent and critical reagent inventories are properly maintained, and that results are properly documented in notebooks and written reports. Complies with Quality Principals related to data generation and reporting and adjusts Quality Systems to match the project stage (e.g. pre-development or development)
Actively participates on cross-functional teams within DSO and GPT and provides support to external departments as time permits. Openly shares scientific expertise and collaboratively helps the team to formulate rational solutions to problems. Shares expertise, instruments and resources within the limitation of established priorities
Maintains a good and current knowledge of the scientific and technical literature pertinent to the project and necessary for development of state of the art production and analytical methods and acquisition of reasonable and necessary equipment
Makes high quality scientific presentations at internal management, regional and national meetings to help advance Allergan’s image as the thought and product leader in the neuromodulator and eye care field. Presents and defends product and process data to regulatory agencies
Makes staffing recommendations related to laboratory staff and communicates desired forward path to management for endorsement/implementation. Evaluates performance for direct reports and assists with staff development via recommendations for internal and external technical training and scientific conferences
Complies with all related environmental health and safety requirements
Skilled in the application of scientific design principles and analytical methodologies to the problems associated with biologicals and/or biopharmaceutical development
Extensive working knowledge and experience with HPLC methods, including SE-HPLC, RP-HPLC, Anion and Cation exchange methods and associated detection systems (UV, fluorescence, etc.)
Experience in CBPA, qPCR and other routine analytical methods including SDS-PAGE, Western Blotting, UV, Bioburden, etc
Excellent instrument skills including HPLC equipment, columns, and associated computers and detection systems, including troubleshooting/problem solving
Proficiency in use of HPLC (Empower, ChemStation, etc.), CBPA/Immunoassay, and statistical software
Experience with development and validation of methods for application within a QC environment
A working knowledge of the requirements of working in a GLP or cGMP environment
Established ability to multi-task
Flexibility - ability to adapt to changing priorities

Associate Director, Pharmaceutical Technology Resume Examples & Samples

Develops and executes process design and test plans to providea technical basis for developing and evaluating new or improved drug product in particular relating to Combination type drug products or modified release implants or patches
Directs the coordination of Drug Product process transfer activities; oversees and approves Drug Product rationalization process and projects in conjunction with Research and Development, Manufacturing, Quality Assurance, and Regulatory Affairs
Provides technical support for investigation and remediation of out of specification results and process deviations for Drug product processes
Serves as technical reviewer of Drug Product related change controls
Provides direction to external CMOs during the design, purchase and validation of new process equipment, both for new and existing manufacturing processes. Defines the Process Validation (PPQ/CPV) requirements resulting from such equipment changes
Leads and executes projects for evaluation and qualification of new sources of excipients and primary packaging components for new and marketed products
Works cross-functionally with Regulatory, Quality, and other departments, as well as internally with Process Technology API colleagues, to implement new API suppliers
Leads or participates in data analysis and interpretation using relevant statistical tools to evaluate experimental results generated as well as production data to improve process control and process robustness
Provides information to support establishing overall budgets, schedules and performance standardsas related to Sterile Drug Product processing operations. Provides direction to meet department objectives
Reports progress of research work and significance of results. Recommends utilization of the results or changes inthe scope of work or termination of projects
Helps determine organizational objectives, and interprets progress of projects. Completed work is reviewed, from a long-term perspective for results
Responsible for training, developing, and advising staff. Accomplishes some results through lower management levels as required
Supports preparation for briefings and technical meetings for top management and interacts with equivalent level staff concerning matters of significance to thecompany
Ensures compliance with all Company policies and procedures, including safety rules and regulations
Travel up to 40%, mostly to Europe and North America
Extensive knowledge of development and bulk manufacturing of Sterile Pharmaceutical drug product and Aseptic processing
Principles and practices of budget preparation and administration
Analytical instrumentation and testing principles and practices relating to sterile drug products
Manufacturing principles as they apply to specialty drug products e.g. Combination type RX/medical devices, drug releasing implants and topical drug delivery patches
Mathematical and statistical computation methods andtechniques
Administration, supervision and training practices and methods
Recruiting, interviewing and selecting applicants in accordance with established employment practices and methods
Current Company policies, practices and procedures, including safety rules and regulations
Responding to complex inquiries frommanagement, employees and regulatory agencies
Formulating and implementing SOPs
Communicating clearly and concisely, both orally and in writing
Managing multiple projects, duties and assignments
Establishingand maintaining cooperative working relationships with others

Manager, Pharmaceutical Compliance Resume Examples & Samples

Creation and maintenance of the Pharma/Dialyzer annual audit schedule and corresponding audit plans based on input provided from management
Create and implement a monitoring program that identifies KPIs for key QSR activities and reports these metrics to management
Ensure adherence to Corporate QS Compliance SOPs and Policies and assuring they are accurate, up-to-date and reflect current practice and reports on ineffective procedures, policy exceptions, reporting discrepancies and evaluates corrective actions and regulatory commitments
Represent the Corporate QS and Clinical Compliance group at meetings
Leads the collection, organization and dissemination of quality knowledge and training about the company, its products, and skills that enable associates to perform their jobs in a continuous state of compliance with applicable regulatory requirements
Tracking of metrics related to audit execution, tracking and closure
Perform audits according to audit schedule and coordinate scheduling of QS and Clinical Compliance activities
Based on results internal process audits, collaborate with Technical Operations, Quality Systems, and GMP Quality functions to identify CAPAs and manage and approve their completion
Contribute to the Quality Management Review
Assist/participate in inspections of FMCNA by Regulatory Authorities
Provide inspection readiness activities throughout the organization including training colleagues across Pharmaceutical organizations on regulatory interactions
Develop internal auditor training program
Interface with internal colleagues, industry leaders and regulatory experts to align audit requirements for FMNCA and provide clarity to the organization of the going-forward support model, as required
Evaluates resource allocations, manages resource and capacity analyses, and oversees the training requirements for direct reports
Participates in continuous improvement efforts to streamline compliance and simplify procedural and other requirements to ensure ease of following system requirements
Provides leadership and coaching to all direct reports and partners with human resources on employee matters
Manage the tactical execution of short- and long-term objectives through the coordination of activities with a direct responsibility for results, including costs, methods, and staffing
Technically proficient in the specific department and knowledge of industry practice and business principles. Works on issues of diverse scope where analysis of situation or data requires evaluation of a variety of factors, including an understanding of current business trends. Has a larger range within the department
Experienced leadership required for multi-faceted environment; role primarily focuses on tactical execution. Receives assignments in the form of objectives and determines how to use resources to meet schedules and goals
Program or project responsibility generally within the function. Manages the operations of one or more departments, direct impact on a specific functional area. Manages the coordination of activities of a section or department with direct responsibility for results, including costs, methods, and staffing. An individual contributor will have significant project/process responsibilities
Follows processes and operational policies in selecting methods and techniques for obtaining solutions. Interprets and recommends change to policies and establishes procedures that effect immediate organization(s)
Decisions have an impact on work processes and outcomes. Erroneous decisions or failure to achieve results will add costs and may impact the short-term goals of the organization
Frequently interacts with subordinate supervisors, customers, and/or functional peer group managers, normally involving matters between functional areas, other company divisions or units, or customers
Participates and presents at meetings with internal and external representatives. Often leading a cooperative effort among members of a project team
Interacts with internal departments and external customers; particularly in problem resolution. Acts as an advisor to subordinate(s) to meet schedules and/or resolve technical problems. Responsible for hiring, coaching and counseling employees, including performance reviews, disciplinary action and terminations
Provide technical guidance
Assist with various projects as assigned
Requisition Management/Pipeline Management which includes candidate screening, as well as database management (consistently reviewing and assessing pipeline for each requisition and dispositioning candidates accordingly)
Manage profitability of Account via development of comprehensive, effective and innovative sourcing and selection strategies in order to efficiently attain top level candidates
Develop process improvements, implement solutions and share best practices with account team members and client partners
Lead weekly meetings with hiring managers and account teams to discuss and assess candidate and requisition status and health. Internet research and job posting responsibility and pipeline status movement
Perform and/or manage passive recruiting through RMS resources as necessary to attract top level candidates
Consult regarding phone interviewing strategies and analysis of completed interviews, including behavioral interviews, of potential candidates to select top level candidates for clients
Accurately forecast and request transitional hours in a timely manner; leverage resources to maximize productivity and pipeline management
Review candidate profile, experience and telephone interview responses and decide final disposition of candidate (i.e.. eligible for hire, not eligible for hire, second round interview eligible, or transfer to another requisition because of skill set match)
Furthermore, sell identified and selected candidates to client hiring managers, as well as advise top level candidates on a client's opportunity including culture fit, knowledge gaps and value proposition
If applicable, negotiate and present compensation packages to candidate for acceptance
Metric analysis, interview guide development, SLA adherence and report generation
Interpret and analyze data and present back to client and account manager so that enhancements can be made to the hiring process such as revisions of behavioral based interview guides, job descriptions, compensation packages, and success indicators
Development and delivery of presentations to client human resource partners and hiring managers
Bachelor's Degree required
3-5 years Experience with a Thorough understanding of recruitment practices
Pharmaceutical recruitment experience
Demonstrated professional growth within HR, Staffing and/or Talent Acquisition Skills and Abilities
Proven ability to design, develop and implement strategic solutions
Ability to interact effectively with all levels of the organization both internally and externally
Technical - Business Knowledge
Demonstrated ability to manage priorities within tight deadlines and high client expectations
Client Focus/Service Orientation
Communication Skills - written and verbal, coupled with interpersonal skills
People Management- embraces the concept of managing up and down
Manages expectations across all levels of the organization and communicates appropriately both internally and externally
ATS System - ability to report and leverage the ATS and manipulate data to share a story internally and externally

Summer Intern, Pharmaceutical Development Resume Examples & Samples

This includes laboratory experimentation for compound characterization, dosage form support and development/optimization of methods
Sample preparation and testing of research compounds on various analytical equipment including HPLC, GC, DSC and dissolution
Effectively document research and to conduct work in a safe manner in accordance with company and departmental guidelines
And other duties as assigned
Must be able to interact with multi level people
Attendance and great time management skills required
Excellent interpersonal skills with strong oral and written communication skills
A basic understanding of biology, physics, organic chemistry and process chemistry as well as current literature
Must be currently enrolled in a relevant science degree program including Chemistry, Biology or Pharmacy and in good academic standing
Must have completed at least one lab and some lab experience helpful
Must be able to lift 50 lbs

Temporary Security Officer Needed for Pharmaceutical Co-flex Shift Resume Examples & Samples

Report safety concerns, security breaches and unusual circumstances both verbally and in writing
Run as needed
Constant mental alertness and attention to detail required while setting priorities and following up on assignments

Late Stage Pharmaceutical Analyst Resume Examples & Samples

Basic understanding of GMP and GLP procedures
Fundamental knowledge of proteins and antibodies; specific experience with protein formulation a plus
Data analysis experience (e.g. Excel, Matlab, Jmp or other programs)
General wet lab skills including protein chromatographic characterization (SEC, IEC, RP), UV-visible spectroscopy and colorimetric assays
Perform analysis of samples with a variety of biochemical and biophysical assays including HPLC, ELSD, icIEF, sub-visible particle counting, osmolality, capillary electrophoresis sodium dodecyl sulfate (CE-SDS)
Prepare data for presentation and assist in generating technical reports, and interact with other groups within the department
Perform review and peer review of analytical data
Troubleshoot method and instrumentation problems as needed
Initiate and perform investigations and development as needed
Develop and execute validation plans as needed
Strong organizational, scientific, computational, communication and interpersonal skills. Highly organized, team oriented, dependable, a self-starter
Knowledge of protein biochemistry is required
Ability to conduct process characterization and validation experiments, design-of-experiment robustness studies, as well as assay qualification studies
Basic to advance analytical knowledge in characterizing proteins with HPLC-based chromatographic techniques, electrophoresis methods, spectroscopy, and other biophysical characterization techniques
Clinical lab experience and GMP/GLP knowledge a plus
Ability to work independently and as part of a team, self-motivated, adaptable and with a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, attention to detail, keep accurate records, follow instructions, and comply with company policies
Bachelor's or Master’s degree in biochemistry, chemistry, analytical chemistry, chemical engineering, or other related degree concentration
1-2 years of industrial experience or 1-2 years of academic research experience

Pharmaceutical Inside Business Development Specialist Resume Examples & Samples

Partner with outside Bio/Pharmaceutical Business Development colleagues to prospect and grow assigned territories
Develop new business revenue for the Bio/Pharmaceutical Division by qualifying and responding to in-coming calls, e-mails, and website inquiries from prospect accounts
Utilize CRM software to manage assigned territory sales funnels. Follow up on assigned opportunities through closure
Transfer new accounts and projects to other teams within Project Management as appropriate
Act as the Project Manager for assigned accounts. Serving as the primary communication link between the client, the laboratory staff, and management
Establish a high client satisfaction rating by quickly responding to all requests, effectively resolving any complaints, setting appropriate expectations, and positioning ELLI for success on all projects
Facilitate client visits to the Lancaster, PA facility
Sales, laboratory, customer service, or project management experience
Strong computer, scientific, organizational, and interpersonal skills
An ability and willingness to learn, perform multiple tasks simultaneously, follow ELLI’s defined sales process, and comply with company policies
Familiarity with the Bio/Pharmaceutical industry
Bachelor's degree in science, marketing/business, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
Authorization to work in the United States indefinitely without restriction or sponsorship

Regulatory Affairs Associate, Pharmaceutical Resume Examples & Samples

You will work on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors
You will be expected to exercise solid judgment in selecting methods, techniques and evaluation criteria for obtaining results
You will add to your knowledge base by networking with key contacts outside your own area of expertise
Ability to influence and partner with cross-functional teams
Ability to take innovative ideas from proof of concept to promote a successful product regulatory strategy and increase probability of regulatory approval
Ability to critically review detailed scientific information and assess whether technical arguments are presented clearly and conclusions are adequately supported by data
Ability to assess project risks, and where appropriate, recommend contingency plans and strategies to mitigate regulatory risks
Demonstrated ability in analytical reasoning and critical thinking skills
Strong capability to contribute and lead in a team environment
Strong business acumen and ability to see the business drivers outside of Regulatory Affairs
Excellent communication skills; both oral and written
Strong interpersonal skills with the ability to influence others in a positive and effective manner through technical excellence and mutual respect
Demonstrated ability to contribute to a continuous learning and process improvement environment
Capacity to react quickly and decisively in unexpected, fluid situations
Detail-oriented with the ability to proofread and check documents for accuracy and inconsistencies
Focused ability to influence operational excellence and performance metrics
A risk averse nature when needed, with the ability to identify potential solutions to complex problems
Authors, coordinates, collects and prepares documentation packages for US drug submissions, periodic updates, and compliance submissions to regulatory agencies. Organizes regulatory information resources and tracks and controls submissions. Reviews and advises on labels, labeling, protocols, and (CMC) changes for compliance with regulatory filings
Under general supervision, collects and coordinates information to prepare regulatory documentation packages for review and submission to regulatory agencies ensuring compliance with all applicable policies, procedures and regulatory requirements and guidelines
Demonstrated working knowledge of scientific principles and domestic regulatory requirements
A self-starter, with the ability to work independently, and as part of a team
Experience working in CMC and post-approval changes desired
Very detail oriented, well organized, and driven to meet deadlines and program goals
Strong verbal and written communication skills including the ability to make effective and persuasive presentations
Strong computer skills with working proficiency of Microsoft Office. Microsoft project and experience with word templates a plus
Prior experience with eCTD submissions preferred. Basic knowledge of CTD required

Digital Producer Pharmaceutical Advertising Resume Examples & Samples

Strong project management skills, understanding of the digital space, including experience with Information Architecture, responsive websites, display campaigns, responsive emails, mobile applications, iPad/Tablet development, and interactive Video
Hands-on involvement in gathering and documentation of business requirements, pre-planning meetings to assess project scope, agency resources, and proper capabilities alignment
Plan timelines and resources, and manage team execution in collaboration with agency peers to ensure project completion on time, on quality and on budget
Develop, drive, and revise timelines, assign resources, manage route and timely approvals for all tactics/deliverables using workflows and follow up directly with resources in person as needed
Manage agency internal resources (strategy, copywriting, design, user experience, development, QA) and contribute ongoing digital insights to ensure digital solutions meet client expectations (KPIs)
Prepare status reports and prioritized hot sheet communications, setup and lead internal meetings, capture internal meeting minutes and next steps, and update all stakeholders as required
Maintain up-to-date and organized files for all stages from concepts to completed pieces
Manage project utilization and review monthly reports, ensure overall project financial health
Evaluate programs to identify potential risks and prepare action plan, implement solutions, document “issues logs”. and escalate appropriately to account and client side management teams
Seek out latest technologies, bringing knowledge of new digital opportunities to internal teams
Excellent listening & communications skills, highly skilled collaborator
Proficient project planning, resource management, quality control
(3-5) years’ experience in digital design & production— some agency experience preferred
Strong understanding of Pharma Campaign Development and Regulatory processes
Understanding of digital best-practices including development technologies, digital trends, digital dreative, web and mobile technology, and how each interacts within the agency process
True problem solver—able to anticipate roadblocks and offer solutions, understand project life-cycle, all dependencies and “ins-and-outs” for each task, able to find ways to facilitate communication and collaboration between departments
Demonstrate curiosity, able to offer new ways of works, and streamlined solutions
Ability to map project information into producing corresponding project timelines from scratch
Working knowledge of Workfront/PHQ, Microsoft (Excel, Word, PPT, Outlook), JIRA, Confluence
Familiarity with creative and web development tools (Photoshop, Illustrator, Indesign, HTML)

Pharmaceutical Network Contract Manager Resume Examples & Samples

Negotiate contracts with pharmaceutical companies and pharmacy distributors in compliance with contract templates, standard checklists, and other key process controls
Review and if necessary, revise contracts
Anticipate and resolve contract language issues
Provide explanation and interpretation of contracts to internal and external customers
Work closely with legal and business teams to ensure contract language accurately conveys intent
Adapt departmental plans and priorities to address business and operational challenges
Establish and maintain strong business relationships with pharmaceutical companies
Participate in additional projects as needed
Identify solutions to non-standard requests and problems
Solve moderately complex problems and/or conduct moderately complex analyses
Work with minimal guidance; seek guidance on only the most complex tasks
Translate concepts into practice
3+ years’ experience as a pharmaceutical contract manager handling complex rebate and procurement agreements with accountability for business results
3+ years’ experience in the pharmaceutical industry
Strong interpersonal skills, establishing rapport and working well with others
Strong negotiation skills
Computer proficiency in Word, Excel
Master's degree
Healthcare, retail pharmacy, or Pharmacy Benefit Management knowledge
Experience working in Industry Relations

Virtual Pharmaceutical Meeting Manager Resume Examples & Samples

Work on special projects as assigned by team leadership
May require travel to destinations worldwide, in support of client site inspections and/or program operations
Handle multiple projects/demands effectively
Ability to communicate effectively and professionally with all levels of management and clients
Neat and professional appearance
Ability to work accurately and timely – in order to meet deadlines
Ability to be flexible and handle change well
Experience with meeting industry technology a plus (CVENT)
Advanced oral and written presentation skills required
Ability to travel by airplane, boat, rail and/or car with travel up to 40%

Marketing Summer Student, Pharmaceutical Resume Examples & Samples

Support analysis on Alivecor pilot project and prepare for phase II of program in the fall based on pilot learnings
Review of Eliquis product promotional material for fall cycle meetings
Assist in building agenda, pre-read and materials for ad boards
Support development of ORP 2.0 (enhancements to be made to the patient support program), specifically related to persistence improvement
Assist in the finalization of tactical plans, planning and cost assessments
Update competitive documents
Prepare VPM slide decks for monthly meetings
Undergraduate degree in commerce, MBA program a plus
B.Sc. degree completed, an asset
Work well in teams, cooperative
Good communication skills in English and French (spoken and written)
Ability to work on different projects at the same time
Good analytical skills and ability to think outside the box
Willing to search for information, challenge and ask questions

Pharmaceutical Project Management Specialist Resume Examples & Samples

Serves as project manager for clients' samples, keeping clients informed of status and TAT and lab informed of client requirements
Balances client needs and satisfaction with internal laboratory requirements for project success (act as advocate to both) and ensures that information is distributed to all who need it
Obtains necessary information for quote preparation and provides to pricing group for quote generation
Audits sample paperwork at required times
Schedules, coordinates and participates in client conference calls, visits and audits; attends meetings with technical groups as needed
Documents client interactions into the project log database
Assess client satisfaction by entering client concerns and complaints into the exception system; works with Group Leader to assist with resolution
Strong computer, scientific, and organizational skills
Excellent communication (oral and written) and attention to detail
Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
Bachelor's degree in science, business, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)

Pharmaceutical Sales Consultant Resume Examples & Samples

Travel via automobile and/or airplane
Valid driver's license with clean driving record and ability to pass a complete background check
Lift and pull up to fifteen (15) pounds
Occasional overnight and/or weekend travel

Director, R&D Quality Brands Pharmaceutical Resume Examples & Samples

Partner with Brands Pharma R&D personnel in developing safe, effective, compliant, and innovative new products and analytical methods
Provide overall guidance and leadership for the Brands Pharma R&D Quality organization
Remain current with legislation and regulatory requirements for product and method development
Quality Leadership responsible for R&D functions supporting Brands pharma activities
Provide quality guidance during all stages of product development lifecycle, including method development/validation, to support agile development of new products/methods
Ensure compliance of Brands Pharma R&D activities to relevant regulatory requirements
Development and maintenance of quality systems for Brands Pharma R&D
Review, approval, and management of documents in support of Brands Pharma R&D
Works with BD&L in due diligence efforts for potential Brands business opportunities, as requested
Provides oversight for Brands Pharma R&D activities performed at CMO’s and/or CRO’s
Works closely with Brands Regulatory Affairs and Pharma R&D to ensure compliance to all relevant marketing authorizations
Ensure safety and regulatory compliance for clinical supplies used in human trials and/or in support of regulatory filings
Ensure regulatory compliance of data generated in the Brands Pharma R&D laboratories in support of regulatory filings
Participate in continuous improvement efforts in support of the Brands business unit
Prepare and host all regulatory authorities during GxP inspections of the Brands Pharma R&D facilities
Ensures all method and process development activities are designed to meet current regulatory requirements when transferred to commercial manufacturing facilities
Represent the quality organization throughout development lifecycle of new products/methods to ensure manufacturability, suitability as well as stability
10 - 15 years related Pharmaceutical experience. Management role with a Quality and/or R&D function in pharmaceutical industry
Expert knowledge of cGMP/GDP, EMA, & ICH requirements/guidelines
Experience working with R&D organizations
Familiarity with new product development lifecycle - including analytical method development
Solid influencing without authority skills
Experience in developing Quality Systems including CAPA, Deviations, and Change control systems
Ability to work independently while still meeting project goals
Strong problem resolution, judgment, and decision making skills
Proven Project Management Experience skills
Ability to Champion regulatory requirements and balance compliance with product requirements
Previous experience in due diligence and integrations activities an advantage
Previous experience working with external manufacturing organizations (CMOs) an advantage
ASQ certified Black Belt and/or Quality Engineer preferred

Pharmaceutical Technology Scientist Resume Examples & Samples

Executes (or supervises) the development and validation of analytical methods using multiple analytical techniques including CBPA, HPLC, qPCR, ELISAs, Western blots, protein content assays, etc. Creates written procedures and protocols. Transfers, qualifies or validates methods as needed. Mentors staff within a matrix environment when needed
Applies routine and specialized analytical techniques to characterize and quantify biopharmaceuticals. Maintains reagent supplies, notebooks, summarizes results in written reports and communicates observations to ensure that the end user receives quality methods in a timely manner. Complies with Quality Principals related to data generation and reporting
Develops protocols and SOPs, trains staff and maintains the laboratory consistent with departmental and Allergan requirements. Understands, documents and adjusts Quality Systems to match the project stage (e.g. pre-development or development)
Makes staffing recommendations related to laboratory staff and communicates desired forward path to management for endorsement/implementation. Evaluates performance for laboratory staff and assists with staff development via recommendations for internal and external technical training and scientific conferences
Extensive working knowledge and experience with CBPA methods, including cell culturing, sterile techniques, cell counting, and ELISA detection systems
Excellent instrument skills including CBPA equipment (CO2 incubators, cell-counting, microscopy and other imaging devices) and associated detection systems (chemiluminescence, electrochemiluminescence, colorimetric, fluorescence detectors)
Proficiency in use of CBPA analysis software (SAS, JMP, Softmax Pro, Gen5, etc.)
Excellent writing and communication skills

Senior Pharmaceutical Scientist / Engineer Resume Examples & Samples

Consistently generates innovative and unique solutions to market needs and submits idea disclosures. Work is expected to result in the development of new or refined products, processes or equipment
Selects techniques to solve complex problems and make sound design recommendations
Assay method development and validation
Release and stability testing at internal and external laboratories
Write CMC sections to support IDE and PMA submissions for combination products
Participate in cross-functional product development teams and provide technical support to sterilization process selection, packaging specification requirements, clinical manufacturing, quality assurance, analytical R&D, and regulatory affairs
The selected candidate must have an ability to collaborate effectively with other scientists in a multidisciplinary team environment and possess excellent verbal and written communication skills
PhD in Pharmaceutical Sciences (Pharmaceutics), Chemistry (Physical, Organic, or Analytical), Biomedical Engineering or related technical field
1-3 years of industry experience in pharmaceuticals under a research and development environment
Understanding and experience in pre-clinical model development
Previous experience with major analytical techniques such as HPLC, GC, LC/MS, GC/MS, and NMR
Experience in practical lab-based Pharmacokinetics/Pharmacodynamics data analysis
Good understanding of cell biology, pharmacology, and biochemistry is highly desirable
Good understanding of controlled drug delivery systems
Good technical writing skills
Deep understanding of pharmaceutics and physical chemistry is a must
Substantial knowledge in assay method development and validation and familiarity with release and stability testing are desirable

Pharmaceutical Procurement Analyst Resume Examples & Samples

Responsible for running all monthly pharmaceutical procurement reports and serve as primary point of contact for questions related to these monthly reports
Maintain all electronic product catalogs with national drug distributors that link to FMS Pharmaceutical Formulary
Update and maintain all catalogs to ensure accurate pricing in all systems
Update all systems including SAP to ensure that FMS facilities have access to purchase the most cost effective Formulary products that are linked to contracted pharmaceutical suppliers
Support Corporate Medical and Clinical Services departments to drive FMS clinics compliance to the FMS drug formulary
Assist Pharma Procurement leaders in review of all available direct and Group Purchasing Contracts to determine the best pricing available by generic drug class for any multi source medications listed on FMS Pharmaceutical Formulary
Conduct daily oversight of the daily SAP Pharma distributor interface
Assist FMS Corporate and Division Finance Centers in resolving any problems encountered with the interface. Follow up with all impacted groups
Serve as a liaison between FMS Finance offices and Corporate SAP IT Team to address any technical issues with the SAP Pharma distributor interface program
Maintain all pharmaceutical contract reporting and provide updates to FMS Finance and other key stakeholders to provide critical senior management reports to track the usage of all ESA and other key medications in use in the NA facilities
Work in collaboration with FMS Supply Chain to maintain and update all pharmaceutical purchase forecast models
Work in collaboration with FMS Corporate Accounting to monitor any pharmaceutical contract rebates earned to ensure accuracy and timeliness of all rebates paid by all contracted suppliers
Validate pharmaceutical sales reports released by national drug distributor against chargeback reports received by all FMCNA contract pharmaceutical supplier. Work with distributor and suppliers to reconcile any sales discrepancies
Work independently to produce analysis and metrics as needed to support all aspects of Pharma Procurement
Provide bid and contract proposal analysis
Performs analysis to support Pharma Procurement projects and collaborate with cross functional teams to ensure all analysis needs are met
Assist with medication related projects including pilots for new medications and roll out of any new drugs added to the FMS Pharmaceutical Formulary
Deal directly with contracted Third Party Logistics (currently ICS) warehouse on all aspects of the ordering and distribution of category specific medications being deployed by FMCNA
Improve and automate existing pharmaceutical analysis and reporting tools and methodologies
Be cross trained in other Pharma Procurement department functions activity to serve as back-up when necessary
Serve as primary backup to Pharmaceutical Customer Service Project Specialist
3 – 5 years of related procurement experience required
Healthcare and/or Pharmaceutical experience a plus
Must have strong Excel skills, and demonstrate a desire to further develop these analytical skills
Technical aptitude and familiarity with the use of Source to Order supply chain systems
Ability to quickly learn company systems including SAP and other inventory replenishment systems
Understanding of financial metrics and their impact on overall profitability
Familiarity with supply chain management concepts
Possess strong problem solving skills
Strong, clear communications skills with the ability to interact with large teams
Strong presentation skills and the ability to present financial statistical data to senior management teams
Able to read, write and verbally articulate pharmaceutical product inventory issues
Ability to comfortably review and present financial information
Able to handle stressful situations without disrupting work performance or projects
Able to support and work in a fast paced team environment
Able to manage tasks on multiple projects in an organized fashion
Preferred - Process improvement, Lean Six Sigma
Project management skills a plus
Coordinate and run daily WMS operations
Meet Productivity Standards
Process, pick, pack, and stage all customer orders when needed
Conduct routine cycle counts upon request
Perform physical inventory counts during semi-annual inventory
Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement”
Customer orientation – establishes and maintains long-term customer relationships, building trust and respect by consistently meeting and exceeding expectations

Related Job Titles

• Conducted thorough inspection of incoming raw materials, resulting in a 15% reduction in defects.
• Maintained detailed documentation for FDA, ISO, and CE mark requirements, ensuring 100% regulatory compliance.
• Devised and implemented Quality Control protocols that enhanced operational efficiency by 20%.
• Managed in-process inspections of intermediate blends, ensuring batch-to-batch consistency.
• Contributed to research projects aimed at characterizing manufacturing materials.
• Maintained a record of 3 years without safety incident or procedural deviation.
• Participated in the launch of a research project investigating medicine optimization.
• Published 2 research papers in internationally recognized chemistry journals.
• Conducted a successful evaluation of a notable test equipment.

5 Quality Control Chemist Resume Examples & Guide for 2024

Customize this resume with ease using our seamless online resume builder.

All resume examples in this guide

Resume Guide

Crafting a stellar quality control chemist resume format, detailing your relevant experience on your quality control chemist resume, decoding the essence of your quality control chemist resume: hard and soft skills, the importance of your certifications and education on your quality control chemist resume, crafting the quality control chemist resume summary or objective: a blend of achievements, aspirations, and uniqueness, extra sections to boost your quality control chemist resume, key takeaways.

One common challenge faced by Quality Control Chemists is effectively communicating their technical skills and specific chemical knowledge on a resume to non-technical hiring managers. Our guide can assist in addressing this issue by providing clear examples and strategies for translating complex chemical concepts and protocols into digestible, impactful language that clearly demonstrates expertise and value to all stakeholders involved in the hiring process.

Enhance your application for the quality control chemist role with our concise guide on how to:

Format your quality control chemist resume, ensuring a balance between professionalism and creativity, in line with best practices.
Align your resume with the quality control chemist job requirements by incorporating relevant industry keywords.
Utilize distinct resume sections to highlight your skills and achievements, making a case for why you're the top pick for the quality control chemist role.
Draw from leading quality control chemist resume examples to effectively tailor your experience.

Upload your resume

Drop your resume here or choose a file . PDF & DOCX only. Max 2MB file size.

functional skill-based resume format - that puts the main focus on your skills and accomplishments;
hybrid resume format - to get the best of both worlds with your quality control chemist experience and skills.

Essential sections for your lead cashier resume, favored by recruiters:

A clear header with pertinent links and contact information.
A concise summary or objective, offering a snapshot of your career milestones and your fit for the lead cashier role.
An experience section detailing your professional qualifications and achievements.
Skills sections that align your talents with job-specific keywords and requirements.
Education and certifications sections that underscore your dedication to industry-specific growth.

What recruiters want to see on your resume:

Education and Credentials: A degree in chemistry or a related field is typically required. Certifications related to quality control, laboratory procedures, or specific types of analysis can also be beneficial.
Technical Skills: Experience with analytical techniques such as HPLC, GC-MS, FTIR, UV/Vis Spectroscopy etc., along with proficiency in using laboratory equipment and software.
Experience in Quality Control: Direct experience in a quality control environment, including performing tests, analyzing results, maintaining documentation, and adhering to safety protocols.
Knowledge of Regulatory Standards: Familiarity with regulatory standards such as GMP, GLP, FDA guidelines, ISO standards, and other relevant industry-specific regulations.
Problem-Solving Skills: Evidence of ability to resolve quality issues, improve processes, and implement changes based on data analysis.
Color on Resume
Resume Icons

Showcase your credibility in the resume experience section. For an effective quality control chemist resume:

Highlight measurable achievements.
Scan the job advert for keywords and integrate them throughout your experience section.
Emphasize your technical proficiencies and how you've applied them in various roles.
Keep it simple: mention your responsibility, relevant skills, and the outcomes.
Use this section to convey your unique value, soft skills, feedback received, and the type of company culture you thrive in.

Top professionals ensure their experience section offers a captivating look at their expertise. Check out our sample quality control chemist resumes for guidance.

Conduct quality control testing on raw materials, intermediate products, and finished goods using analytical techniques such as HPLC, GC, and spectroscopy.
Develop and validate analytical methods to ensure accurate and reliable results, improving overall efficiency by 20%.
Collaborate with cross-functional teams to investigate and resolve product non-conformance issues, resulting in a 15% reduction in customer complaints.
Perform stability studies to assess the shelf life of products, implementing new protocols that extended product expiration dates by six months.
Maintain and calibrate laboratory equipment, ensuring compliance with industry standards and regulations.
Executed quality control tests on incoming raw materials, documenting results and providing feedback to suppliers, resulting in a 10% improvement in material quality.
Led a team in the implementation of a new quality management system, streamlining processes and reducing product release time by 30%.
Investigated out-of-specification test results and implemented corrective actions, ensuring compliance with regulatory requirements.
Conducted validation studies for new manufacturing processes, contributing to the successful launch of three new products.
Performed routine audits of manufacturing areas and identified opportunities for process optimization, resulting in a 25% increase in overall productivity.
Performed analytical testing on samples using techniques such as titration, pH measurement, and viscosity determination.
Assisted in the development and optimization of analytical methods, reducing analysis time by 20%.
Supported process improvement initiatives by identifying root causes of quality issues, leading to a 15% reduction in production defects.
Collaborated with R&D teams to transfer new products from development to manufacturing, ensuring smooth scale-up processes.
Participated in internal and external audits, addressing findings and implementing corrective actions to maintain compliance.
Conducted routine analysis of raw materials, intermediate products, and finished goods, following established protocols and specifications.
Maintained accurate documentation of test results and performed data analysis, reporting any deviations or trends to management.
Collaborated with production teams to investigate and resolve process-related quality issues, resulting in a 10% reduction in reject rates.
Assisted in the training of new laboratory personnel on analytical techniques and quality control procedures.
Implemented statistical process control methods to monitor key quality parameters, improving process stability by 20%.
Performed physical and chemical tests on samples, including moisture content, particle size analysis, and identification of impurities.
Assisted in the development of standard operating procedures (SOPs) for quality control testing, ensuring consistent practices.
Conducted investigations into out-of-specification results, identifying root causes and implementing corrective actions.
Collaborated with the purchasing department to evaluate potential suppliers and assess their product quality and reliability.
Maintained laboratory equipment and reagent inventory, ensuring proper functioning and availability of necessary supplies.

Quantifying impact on your resume

Include the number of QC procedures developed and implemented, demonstrating your ability to create efficient workflows.
List the percentage of reduction in non-compliance incidents following your interventions, showing your impact on regulatory adherence.
Report the number of analytical methods you've optimized or newly introduced, showcasing innovation and process improvement skills.
State the frequency of audits performed and their successful outcomes, highlighting your diligence and commitment to quality.
Mention the figure related to savings achieved through cost-effective laboratory practices, indicating business value creation.
Quantify the amount of training sessions provided to junior chemists, emphasizing leadership and team-building capabilities.
Present the number of times you've identified and addressed deviations from Standard Operating Procedures (SOPs), reflecting problem-solving skills and attention to detail.
Enumerate any significant increase in yield or efficiency due to your contributions, proving your effectiveness in driving productivity.

Addressing a lack of relevant quality control chemist experience

Even if you lack direct quality control chemist experience, you can still craft a compelling resume. Here's how:

Highlight projects or publications that demonstrate your relevant skills or knowledge.
Emphasize transferable skills, showcasing your adaptability and eagerness to learn.
In your objective, outline your career aspirations and how they align with the company's goals.
Consider a functional or hybrid resume format, focusing on skills over chronological experience.
How to Write Your First Job Resume Guide
Job Shadowing on Resume

Ensure your quality control chemist experience descriptions resonate with both tech-savvy and non-tech audiences. Adopting a consistent format, such as task-action-result, can lend clarity and coherence to your experience section.

Every job description communicates the desired hard and soft skills. These skills are the backbone of your application.

Hard skills are your tangible, technical proficiencies, often validated through certifications or hands-on experience. On the other hand, soft skills reflect your interpersonal abilities and how you navigate diverse work environments.

To effectively spotlight these skills on your resume:

Create a distinct section for technical skills, listing the most relevant ones for the job.
Highlight your strengths by weaving in achievements that underscore specific skills.
Strike a balance between hard and soft skills to present a well-rounded profile.
If multilingual, include a language proficiency section, emphasizing the interpersonal advantages it brings.

Stay tuned for a deep dive into the most in-demand hard and soft skills in the industry.

Top skills for your quality control chemist resume

Analytical Chemistry

Spectroscopy

Chromatography

Lab Safety Procedures

Quality Assurance & Control

Experimental Design & Analysis

Chemical Testing & Analysis

Good Manufacturing Practices (GMP)

Documentation & Record Keeping

Statistical Process Control

Attention to Detail

Problem Solving

Communication Skills

Time Management

Critical Thinking

Adaptability

Decision Making

Organizational Skills

Targeting the needed job ad skills doesn't have to end with the skills section. You can talk about your related certifications, interests or additional experience via projects or volunteering, where you picked up those skills, too.

Pay attention to the resume education section . It can offer clues about your skills and experiences that align with the job.

List only tertiary education details, including the institution and dates.
Mention your expected graduation date if you're currently studying.
Exclude degrees unrelated to the job or field.
Describe your education if it allows you to highlight your achievements further.

Your professional qualifications: certificates and education play a crucial role in your quality control chemist application.

They showcase your dedication to gaining the best expertise and know-how in the field.

Include any diplomas and certificates that are:

Listed within the job requirements or could make your application stand out
Niche to your industry and require plenty of effort to obtain
Helping you prepare for professional growth with forward-facing know-how
Relevant to the quality control chemist job - make sure to include the name of the certificate, institution you've obtained it at, and dates

Both your certificates and education section need to add further value to your application.

That's why we've dedicated this next list just for you - check out some of the most popular quality control chemist certificates to include on your resume:

Best certifications to list on your resume

Certified Quality Engineer (CQE) - American Society for Quality (ASQ)
Certified Quality Auditor (CQA) - American Society for Quality (ASQ)
Six Sigma Black Belt Certification (CSSBB) - American Society for Quality (ASQ)
Certified Reliability Engineer (CRE) - American Society for Quality (ASQ)
ICH Quality Guidelines Certificate - International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)
ISO 9001:2015 Quality Management Systems certificate - International Organization for Standardization (ISO)
Clinical Laboratory Scientist Certificate (CLS) - American Association for Clinical Chemistry (AACC)

Listing your relevant degrees or certificates on your quality control chemist resume is a win-win situation. Not only does it hint at your technical capabilities in the industry, but also at a range of soft skills, including perseverance, adaptability, and motivation.

GPA on Resume
Cum Laude on Resume

Whether you opt for a resume summary or objective depends on your career trajectory.

If you have a rich tapestry of relevant achievements, a resume summary can spotlight these accomplishments.
If you're relatively new or transitioning, a resume objective can articulate your aspirations and how they align with the role.

Regardless of your choice, this section should encapsulate your unique value proposition, blending your technical and interpersonal strengths.

Resume summary and objective examples for a quality control chemist resume

Seasoned chemist with 10 years of experience, specializing in quality control. Proficient in analytical tools such as HPLC, GC, and FTIR. Recognized for increasing laboratory efficiency by 20% through upgrading protocols at XYZ Corp.
Accomplished analytical chemist, credited with improving product purity by 15% over a 5-year tenure at ABC Corporation. Comprehensive knowledge of spectroscopy and chromatography techniques, with an emphasis on developing robust testing procedures.
Professional software engineer transitioning to a quality control chemist role. Armed with a master’s degree in chemistry and extensive data analysis skills. Successfully implemented a machine learning algorithm to predict chemical reactions in a recent project.
Experienced mechanical engineer ready to apply transferable skills to a career in quality control chemistry. Holds a bachelor's degree in Chemical Engineering. Proven ability to improve system efficiency, with an achievement of reducing production downtime by 25% in DEF Industries.
A recent chemistry graduate eager to commence a career in quality control. Strong academic background in analytical techniques and laboratory protocols. Driven to optimize efficiency and elevate the standards of chemical product validation.
Newly graduated biochemist aiming to utilize strong laboratory skills in a quality control environment. Keen interest in pharmaceutical industry regulations and best practices. Committed to contributing to the high standard of integrity in chemical analysis and testing.

Recruiters love candidates who offer more. Share your personality or extra industry credentials. Consider adding:

Projects showcasing standout work.
Top awards or recognitions.
Relevant publications .
Hobbies and interests that reveal more about you.
Your resume's layout should be both visually appealing and content-rich.
Emphasize achievements that resonate with the job's requirements.
Detail your skills, both technical and interpersonal, with real-world examples.
Ensure the top section of your resume provides a clear snapshot of who you are and what you offer.
When detailing experience, focus on tasks, actions, and their outcomes.

Looking to build your own Quality Control Chemist resume?

Resume Examples

Why and How to Write a Resignation Email (With Examples)

Resume after career break, interview question: tell me what you know about our company, do you have to list all your jobs on an application, how to write a modern resume, negotiating a salary increase for a new job: what to expect and how to ask.

Create Resume
Terms of Service
Privacy Policy
Cookie Preferences
Resume Templates
AI Resume Builder
Resume Summary Generator
Resume Formats
Resume Checker
Resume Skills
How to Write a Resume
Modern Resume Templates
Simple Resume Templates
Cover Letter Builder
Cover Letter Examples
Cover Letter Templates
Cover Letter Formats
How to Write a Cover Letter
Resume Guides
Cover Letter Guides
Job Interview Guides
Job Interview Questions
Career Resources
Meet our customers
Career resources
English (UK)
French (FR)
German (DE)
Spanish (ES)
Swedish (SE)

Made with love by people who care.

Top 18 Pharmacy Manager Resume Objective Examples

Updated July 11, 2023 14 min read

A resume objective is a brief statement at the top of your resume that summarizes your professional goals and highlights your qualifications as they relate to a specific job. It should be tailored to the position you are applying for, and should make it clear why you are the ideal candidate for the role. When writing a resume objective for a pharmacy manager position, focus on your experience managing pharmacies, including any relevant certifications or training. Additionally, emphasize any leadership qualities you possess that would make you an effective leader in this role. For example, “Highly organized pharmacy manager with 10 years of experience and certification in retail pharmacy management seeking to lead an innovative team at ABC Pharmacy.” By clearly expressing your career aspirations and qualifications, a well-crafted resume objective can help you stand out from other applicants.

or download as PDF

Top 18 Pharmacy Manager Resume Objective Samples

To secure a position as a Pharmacy Manager and utilize my expertise in pharmaceuticals, customer service, and management.
To obtain a Pharmacy Manager role with an organization that values dedication and commitment to patient care.
Seeking a position as a Pharmacy Manager where I can use my knowledge of pharmaceuticals, operational management, and customer service to contribute to the success of the organization.
To work as a Pharmacy Manager in an environment that rewards innovation and hard work.
Looking for an opportunity to leverage my experience in pharmacy operations and customer service to provide exceptional patient care as a Pharmacy Manager.
To bring my knowledge of pharmacy operations, inventory management, and customer service to the position of Pharmacy Manager.
To obtain a challenging position as a Pharmacy Manager where I can utilize my skills in pharmaceuticals, inventory management, and customer service.
Seeking an opportunity to apply my knowledge of pharmacy operations and customer service to contribute to the success of an organization as a Pharmacy Manager.
Looking for a position as a Pharmacy Manager where I can use my experience in pharmaceuticals, inventory control, and customer service to provide excellent patient care.
Aiming for the role of Pharmacy Manager at an organization that values quality patient care and professionalism.
To utilize my experience in pharmacy operations and customer service in order to become an effective leader in the field of pharmacy management.
Seeking employment as a Pharmacy Manager with an organization that emphasizes quality patient care while maintaining high standards of professionalism.
Aiming for the role of Pharmacy Manager at an organization that values excellence in patient care while providing superior customer service.
To obtain employment as a Pharmacy Manager utilizing my expertise in pharmaceuticals, inventory control, and customer service while delivering quality healthcare services.
Seeking employment at an organization where I can apply my knowledge of pharmacy operations, inventory control, and customer service while providing exceptional patient care as a Pharmacy Manager.
Looking for an opportunity to use my experience in pharmaceuticals, operational management, and customer service within the role of Pharmacy Manager at an established healthcare facility.
Aiming for the role of Pharmacy Manager with an organization that emphasizes excellence in patient care while maintaining high standards of professionalism.
Seeking employment as a Pharmacy Manager with an established healthcare facility utilizing my expertise in pharmaceuticals, inventory control, operational management, and customer service while providing quality healthcare services

How to Write a Pharmacy Manager Resume Objective

A pharmacy manager resume objective is a statement which outlines an individual’s career goals and qualifications for a position as a pharmacy manager. It should be concise yet detailed enough to capture the attention of potential employers and make them want to learn more about the applicant. Crafting an effective resume objective can be challenging, but with careful consideration and preparation it can be done successfully.

When writing a pharmacy manager resume objective, it is important to focus on your qualifications relevant to the job. You should include any previous experience that you have in the field, such as working as a pharmacist or in another related role. Additionally, you should highlight any special skills that you possess that make you unique from other applicants, such as knowledge of medical terminology or familiarity with certain software programs. Your objective should also include any educational qualifications that are relevant to this role, such as a degree in pharmacy management or healthcare administration.

In addition to listing your qualifications, you should also describe what you hope to accomplish in this role. For example, if you have experience in managing pharmacies with multiple locations, your objective could state something like “seeking a position as a pharmacy manager where I can utilize my experience managing multiple locations and maximize customer satisfaction”. This will demonstrate your enthusiasm for the job and show employers that you are motivated to succeed in this position.

Finally, when writing your pharmacy manager resume objective it is important to keep it concise yet informative. Be sure to avoid cliches or overly generic phrases such as “seeking an opportunity” or “ready for new challenges”- instead focus on what makes you uniquely qualified for this position and how you plan on succeeding within it. With these tips in mind, crafting an effective pharmacy manager resume objective will help set yourself apart from other candidates and make your application stand out from the rest!

Related : What does a Pharmacy Manager do?

Key Skills to Highlight in Your Pharmacy Manager Resume Objective

Crafting a compelling resume objective is crucial when applying for the position of a Pharmacy Manager. This section should not only express your career goals but also highlight your key skills that make you an ideal candidate for the role. The objective serves as a brief yet powerful statement that can set the tone for the rest of your resume. In this section, we will discuss some essential skills to emphasize in your pharmacy manager resume objective, which can significantly enhance its impact and increase your chances of securing an interview.

1. Inventory management

A Pharmacy Manager is responsible for overseeing and managing the operations of a pharmacy, which includes maintaining an accurate inventory of medications and pharmaceutical supplies. Inventory management skills are essential in this role to ensure that the pharmacy is always stocked with necessary items, avoid overstocking or under-stocking situations, manage costs effectively, and prevent losses due to expired or damaged goods. This skill also helps in predicting future needs and making timely orders. Including this skill in a resume objective shows potential employers that the candidate can efficiently handle these responsibilities, leading to smooth pharmacy operations.

2. Staff supervision

A Pharmacy Manager is responsible for overseeing and managing the operations of a pharmacy, which includes supervising staff. This skill is needed for a resume objective to demonstrate the ability to effectively lead a team, ensure tasks are completed accurately and efficiently, and maintain a high standard of service. It also shows potential employers that the candidate can handle responsibility, make important decisions, and resolve any staff-related issues that may arise.

3. Patient counseling

A Pharmacy Manager not only oversees the operations of a pharmacy but also interacts directly with patients. Patient counseling is a crucial skill as it involves educating patients about their medications, explaining how they work, potential side effects, and answering any queries they may have. This skill is necessary to ensure patient safety and satisfaction, which in turn contributes to the success and reputation of the pharmacy. Including this skill in a resume objective demonstrates the candidate's ability to effectively communicate complex medical information to patients and provide excellent customer service.

4. Medication dispensing

A Pharmacy Manager is responsible for overseeing the operations of a pharmacy, which includes the accurate dispensing of medications. This skill is crucial as it ensures that patients receive the correct medication in the proper dosage, contributing to their health and safety. Including this skill in a resume objective demonstrates the candidate's ability to perform one of the key functions of the job effectively and accurately. It also shows their knowledge and understanding of various medications, attention to detail, and commitment to patient care.

5. Regulatory compliance

A Pharmacy Manager is responsible for overseeing the operation of a pharmacy, ensuring that all practices are in line with regulatory standards. Having a skill in regulatory compliance demonstrates an understanding and adherence to laws, guidelines, and specifications relevant to their role. This can include areas such as dispensing medication, record-keeping, and patient privacy. This skill is crucial as it helps prevent legal issues, ensures the safety and health of patients, maintains the pharmacy's reputation, and contributes to efficient and effective management. Therefore, highlighting this skill in a resume objective can show potential employers that the candidate is capable of managing a pharmacy within the required legal framework.

6. Financial oversight

A pharmacy manager is responsible for the financial health and profitability of the pharmacy. They need to manage budgets, control inventory, and make decisions about purchasing and pricing. Financial oversight skills are crucial for ensuring the pharmacy operates within its means, maximizes profits, and continues to provide excellent service to its customers. Including this skill in a resume objective demonstrates an understanding of the financial responsibilities associated with managing a pharmacy and shows potential employers that you have the ability to successfully handle these tasks.

7. Workflow optimization

A Pharmacy Manager is responsible for overseeing and managing the operations of a pharmacy. This includes ensuring that all tasks are completed efficiently and effectively. Workflow optimization skills are crucial as they allow the manager to streamline processes, improve productivity, reduce errors and waste, and ensure that the pharmacy runs smoothly. This skill demonstrates the ability to increase efficiency in a pharmacy setting, which can lead to improved customer service, reduced costs, and increased profitability. Therefore, highlighting this skill in a resume objective can make a candidate more appealing to potential employers.

8. Quality assurance

A Pharmacy Manager is responsible for overseeing and managing the operations of a pharmacy, ensuring that all medications are stored and dispensed correctly. Quality assurance is a critical skill in this role as it involves monitoring and maintaining the highest standards of accuracy and safety in dispensing medication. This skill is necessary to prevent errors, ensure patient safety, comply with regulations, and maintain the reputation of the pharmacy. Including quality assurance in a resume objective shows potential employers that the candidate is committed to high standards of practice and patient care.

9. Conflict resolution

A Pharmacy Manager often needs to handle disputes or disagreements between staff members, customers, or suppliers. Conflict resolution skills are crucial in maintaining a harmonious work environment and ensuring customer satisfaction. It also helps in making effective decisions during stressful situations, preventing any potential negative impact on the pharmacy's operations or reputation. Including this skill in a resume objective can highlight the candidate's ability to manage challenging situations efficiently and maintain a positive workplace culture.

10. Customer service

A Pharmacy Manager needs strong customer service skills because they interact directly with patients, healthcare providers, and staff. They need to provide clear communication, handle complaints, and ensure a high level of patient care. This skill is crucial in maintaining a positive environment, improving patient satisfaction, and ensuring the smooth operation of the pharmacy. Including this skill in a resume objective shows potential employers that the candidate understands the importance of providing excellent service to all stakeholders.

Top 10 Pharmacy Manager Skills to Add to Your Resume Objective

In conclusion, the objective section of your Pharmacy Manager resume presents a crucial opportunity to showcase your key skills. It is essential to carefully select and highlight those abilities that align with the job requirements and demonstrate your capacity to excel in this role. This not only sets the tone for the rest of your resume but also helps potential employers quickly identify you as a strong candidate. Remember, an effective resume objective can be instrumental in setting you apart from other applicants and securing that coveted interview.

Related : Pharmacy Manager Skills: Definition and Examples

Common Mistakes When Writing a Pharmacy Manager Resume Objective

Writing a resume objective for a pharmacy manager position can be challenging, as it requires distilling your experience and qualifications into just a few sentences. However, there are certain common mistakes to avoid when crafting this important part of your resume.

The first mistake to avoid is writing an objective that is too general or vague. A generic statement such as “seeking a pharmacy manager role” does not provide any information about what makes you a qualified candidate for the position. Instead, focus on specific skills and experiences which make you stand out from other applicants. For example, “Seeking a pharmacy manager role where I can leverage my ten years of pharmacy management experience and my expertise in medication safety protocols to help improve patient care outcomes.”

Another mistake to avoid is including irrelevant information in your resume objective. It is important to only include relevant information that demonstrates why you are the best candidate for the job. Generic statements such as “I am hardworking and reliable” do not provide useful information about your qualifications and can instead detract from your overall message.

Finally, it is important to avoid using overly technical language in your resume objective. While some technical terms may be appropriate depending on the position, try to keep most of the language straightforward and reader-friendly. This will ensure that employers understand the value you bring to their organization without having to decipher complex terminology or jargon.

By avoiding these common mistakes when writing your resume objective for a pharmacy manager position, you will be able to create an effective summary of your qualifications that stands out from other applicants and highlights why you are the best fit for the job.

Related : Pharmacy Manager Resume Examples

Pharmacy Manager Resume Objective Example

A right resume objective for a pharmacy manager would focus on the desired skills and qualifications needed for the position, while a wrong resume objective would simply list unrelated goals or aspirations.

Editorial staff

Brenna Goyette

Brenna is a certified professional resume writer, career expert, and the content manager of the ResumeCat team. She has a background in corporate recruiting and human resources and has been writing resumes for over 10 years. Brenna has experience in recruiting for tech, finance, and marketing roles and has a passion for helping people find their dream jobs. She creates expert resources to help job seekers write the best resumes and cover letters, land the job, and succeed in the workplace.