Job Overview
Location
United States Remote Office
Job Type
Full-time
Category
Product Management
Date Posted
July 9, 2026
Full Job Description
đź“‹ Description
- • Direct all aspects of nonclinical development including staffing, supervising, providing work direction, goal setting, prioritization, etc.
- • Oversee the development of the nonclinical regulatory strategy, design of experiments, interpretation of data and oral and written presentation of results.
- • Oversee the review and approval of all preclinical protocols and final reports for nonclinical development studies and ensure data quality and integrity for preclinical sites.
- • Effectively communicate preclinical findings to project teams, senior management, regulators and other external partners.
- • Oversee the research and construction of regulatory study documents for new and complex product development (i.e., IND/NDA preclinical sections etc.).
- • Represent Viatris and Global Pharmacology and Toxicology in meetings with regulatory agencies.
- • Provide technical support to various departments within the company with respect to pharmacology and toxicology.
- • May perform and serve as a reviewer on toxicological risk assessments for various health based exposure limits (HBELs), such as ADEs, PDEs, ADIs and OELs.
- • Assist in the development and adherence to departmental budget.
- • Review for comprehension relevant Standard Operational Procedures (SOPs).
🎯 Requirements
- • Minimum of a Bachelor's degree (or equivalent) and 15 years of experience. DVM, PhD or in a biomedical discipline or PharmD degree preferred with 10 years of relevant pharmaceutical experience preferred.
- • Must possess expert knowledge of pharmaceutical drug development requirements for regulatory submissions.
- • Must possess expert in-depth knowledge of product development, analytical sciences, and clinical operations.
- • Must have broad knowledge of GMP, GLP, GCP and the Global Regulatory process for Brand/Specialty and generic product approval.
- • Ability to read and interpret comprehensive and intricate research documents.
- • Ability to write scientific reports and technical correspondence.
🏖️ Benefits
- • Competitive salaries
- • Benefits
- • Inclusive environment
- • Opportunity to make an impact on the lives of others
- • Equal Opportunity Employer
- • Salary range for this position is $151,000 - $314,000
Skills & Technologies
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About Viatris Inc.
Viatris Inc. is a global healthcare company formed in 2020 through the combination of Mylan and Upjohn, a legacy division of Pfizer. It develops, licenses, manufactures, markets and distributes a broad portfolio of branded, generic, complex generic, biosimilar and over-the-counter medicines, as well as active pharmaceutical ingredients. The company operates in more than 165 countries and territories, focusing on expanding access to medicines for non-communicable and infectious diseases, driven by a Global Healthcare Gateway that leverages its supply-chain, scientific and regulatory expertise to serve patients worldwide.
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