Senior Formulation Scientist

1100 Mylan Pharmaceuticals Inc.; Morgantown (WV); On-site; USD 90,000 - 120,000; Full time

Job summary

Viatris seeks a Senior Formulation Scientist to provide technical support for tech transfer and develop scalable formulations for new and existing products. You will review protocols, track progress, and prepare regulatory documents while ensuring cGMP and safety standards are met.

The role requires a strong foundation in solid oral dosage form development, process optimization and cross-functional collaboration within a manufacturing and development environment.

Qualifications

• Bachelor's degree (or equivalent) with 2–4 years of experience; higher degrees with more experience are preferred.
• Experience with generic drug development is desirable.
• Strong understanding of solid oral dosage form development, process optimization, and scale-up.

Responsibilities

• Provide technical support of tech transfer activities for existing products.
• Review proposals, timelines, protocols, manufacturing documents, test results and reports.
• Track project progress and provide timely updates to key stakeholders.
• Manufacture experimental batches and support tech transfer qualification batches.
• Troubleshoot problems during tech transfer activities.
• Prepare and review technical regulatory documents for tech transfer submissions.
• Design formulations and processes for new products and support development, optimization and scale-up.
• Keep current with cGMP, SOPs, FDA regulations and safety.
• Attend training to maintain and increase skills and knowledge.

Skills

Formulation development

Process optimization

Scale-up

Technical writing

Communication

Teamwork

MS Office

Excel

Statistics

Pharmacokinetics

Education

Pharmaceutics

Chemical Engineering

Chemistry

Related field

Tools

MS Office

Job description

Mylan Pharmaceuticals Inc. Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases. We have been included on number of award lists that demonstrate the impact we are making.

Every day, we rise to the challenge to make a difference and here's how the Senior Formulation Scientist will make an impact:

Key responsibilities for this role include:

• Provide technical support of tech transfer activities for existing products.
• Review proposals/timelines, protocols, manufacturing documents, test results and reports for tech transfer projects.
• Track project progress and provide timely updates to key stakeholders.
• Manufacture experimental batches in support of tech transfer activities and provide support during the manufacture of tech transfer qualification batches.
• Troubleshoot any problems that occur during tech transfer activities.
• Prepare and review technical regulatory documents in support of tech transfer submissions.
• Design formulations and processes for new products and manufacture development, optimization and scale-up batches for new products.
• Keep current with all Federal guidelines, compendial requirements, technical innovations, and topics of current interest pertaining to projects.
• Attend training sessions in order to maintain and increase skills and knowledge of cGMP's and safety awareness.

The minimum qualifications for this role are:

• Minimum of a Bachelor's degree (or equivalent) and 2-4 years of experience.
• A Bachelor's degree and 7 years of experience, a Master's degree with 5 years of experience or a doctorate with 0-2 years' experience preferably in the pharmaceutical industry or related scientific field is preferred.
• Degrees in Pharmaceutics, Chemical Engineering, Chemistry or related scientific fields are preferred.
• However, a combination of experience and/or education will be taken into consideration.
• Experience with generic drug development desirable.
• Demonstrates comprehensive understanding of solid oral dosage form development, process optimization and scale-up.
• Must understand the pharmacokinetics of drugs.
• Must have working knowledge of cGMPs, Standard Operating Procedures, FDA regulations and safety.
• Must possess strong writing, communication, comprehension, interpretation, problem solving, team, critical thinking, and organization skills.
• Must possess the ability to use creativity to solve formulation problems and make sound decisions in manufacturing situations.
• Must possess excellent technical computer skills including MS Office Suite.
• Ability to read and interpret complex business and/or technical documents.
• Ability to write comprehensive reports and detailed business correspondence.
• Ability to work with managers or directors and communicate ambiguous concepts.
• Ability to present to groups across the organization.
• Ability to add, subtract, multiply, divide and perform statistical computations.
• Advanced mathematical skills preferred.
• Familiarity using formulas in Microsoft Excel preferred.
• Ability to solve problems with a variety of concrete variables through semi-standardized solutions that require some ingenuity and analysis.
• Ability to draw inferences and follow prescribed and detailed procedures to solve moderately complex problems.

May be required to stand; walk; stoop; bend; kneel; and climb steps. May require use of hands and use of arms to lift and scoop. May be required to lift or maneuver boxes or containers using lifting equipment, as well as physically pushing, rolling or lifting. May be required to wear personal protective equipment including but not limited to: respiratory protection, safety glasses, hearing protection, safety shoes and protective clothing. Light to medium lifting requirements. Travel is required as needed. Laboratory, pilot and production plant, and office environments. Working alone or closely with others. The work environments can be described as laboratory to light manufacturing/pilot plant. Part of the work day may be spent in a typical office environment.

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, gender expression, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.

Viatris is a global healthcare company formed in 2020 through the combination of Mylan and Upjohn, a legacy division of Pfizer. By integrating the strengths of these two companies, including our global workforce, we aim to deliver increased access to affordable, quality medicines for patients worldwide, regardless of geography or circumstance. We believe in healthcare as it should be - empowering people worldwide to live healthier at every stage of life. Because of our unwavering belief that better access leads to better health, we leverage our best-in-class manufacturing and scientific expertise and proven commercial capabilities to bring quality medicines to patients when and where they need them.