QA Specialist II
Gilead Sciences · Foster City, CA
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Role summary
This QA Specialist II role supports quality oversight of small molecule drug substance and oral solid dosage manufacturing at a clinical stage. Responsibilities include reviewing manufacturing documentation, maintaining GMP records, conducting risk-based investigations, and supporting process improvement and regulatory activities. Candidates need 4+ years of GMP experience with a BS degree, or 2+ years with an MS degree.
Privacy & handoff
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