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Location
In office (Morgantown)
Seniority
Junior · 2+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 11, 2026. First seen by Alion on Nov 11, 2026. Viatris scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Viatris is a global pharmaceutical company headquartered in Canonsburg, Pennsylvania, that develops, manufactures and sells generic, branded and complex medicines. It was formed in November 2020 through the merger of Mylan, founded in 1961 in West Virginia, with Upjohn, the off-patent medicines division of Pfizer, and supplies medicines to about 1 billion patients a year from sites in the United States, Ireland, India, Hungary and other countries. Viatris hires pharmaceutical sales representatives, analytical and material scientists, sterile product and manufacturing engineers, finance analysts, data scientists and marketing staff.
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 Lead Formulation Scientist will make an impact:

Key responsibilities for this role include:

  • Design formulations and processes for new products and manufacture development, optimization and scale-up batches for new products.
  • Evaluate product testing results and finalize production formulations and processes.
  • Troubleshoot any problems that occur during scale-ups or in production.
  • Write tech transfer reports, development reports and other technical regulatory documents for new product submissions.
  • Provide technical support of tech transfer activities for existing products.
  • Report project status (development plans, timelines) to supervisor.
  • 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.
  • Perform other duties as assigned.

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 5 years of experience, a Master’s degree with 2 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 basic principles of 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.

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