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Job description
Revolution Medicines, a late-stage clinical oncology company, seeks an Associate Director for GMP Quality Assurance to oversee DS/DPI batches, ensure GMP compliance, and support CMC submissions. You will partner with Technical Operations and CDMOs to maintain quality and inspection readiness for clinical and commercial programs.
Ideal candidates bring 10+ years in GMP quality, strong risk assessment and leadership, and experience with DS/DPI manufacturing, validation, and regulatory filings.
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Worksite address
san francisco, CA, 94199, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.