Sr Manager, Regulatory Affairs CMC

Gilead Sciences(5 days ago)

United States, California, Foster City, CAOnsiteFull TimeSenior$157,590 - $203,940Regulatory Affairs

About this role

The CMC Regulatory Affairs Project Manager at Gilead supports the planning, coordination, and execution of regulatory activities related to pharmaceutical development and commercialization. The role involves collaboration across various teams and managing global submissions to health authorities, contributing to the development of life-changing therapies.

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Required Skills

Regulatory Affairs
Project Management
CMC
Pharmaceutical Development
Documentation
Cross-functional Collaboration
Quality Assurance
Regulatory Submissions
Stakeholder Engagement
Analytical Methods

Qualifications

Bachelor’s degree in Life Sciences, Chemistry, Pharmacy, or related discipline
4-6+ years of relevant experience in pharmaceutical project, CMC development, or CMC Regulatory Affairs

About Gilead Sciences

gilead.com

Gilead Sciences is a biopharmaceutical company dedicated to transforming patient care by advancing therapeutics in areas like HIV, liver disease, cancer, and inflammation. With a strong commitment to innovation, Gilead leads in the research and development of new medicines, aiming to make the world a healthier place. Their portfolio includes breakthrough therapies and ongoing advancements across multiple therapeutic areas, supported by a robust pipeline of clinical trials. Gilead is recognized for its contributions to public health and its efforts to improve access to vital medications.

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