Olema Oncology is seeking an Associate Director, GMP Quality to oversee GMP activities for clinical and commercial products, including QA review of batch records and supplier compliance. This role partners with CMC, Regulatory and Supply Chain, and will be based in SF or Boston with travel.
The ideal candidate has 8+ years in FDA-regulated pharma GMP QA, experience with NDA/BLA submissions, and strong leadership and communication skills.
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