Senior CMC Regulatory Lead Biopharma Development
Listed on 2026-10-08
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Pharmaceutical
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Healthcare
GSK in the United States seeks a senior CMC regulatory lead to drive global submission strategies for investigational, late development and early commercial products. You will collaborate with chemistry, manufacturing and quality teams to ensure timely and compliant documentation.
You will mentor staff, engage with regulators, and lead major inspections. The role offers broad responsibility within a multinational biopharma environment, with competitive compensation and benefits.
The Senior CMC Regulatory Lead for Biopharma Development position in the Bio & Pharmacology & Health, Management & Operations field is open for applications.
Learn more about the Senior CMC Regulatory Lead for Biopharma Development role in the description above.
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