Olema Oncology is seeking an Associate Director, GMP Quality to oversee GMP activities for clinical and commercial products, including review of batch records and supplier compliance. The role requires collaboration with CMC, Regulatory, and Supply Chain functions and may involve visits to CMOs.
Based in San Francisco or Boston with 10–15% travel. The ideal candidate has a strong background in FDA-regulated GMP QA, NDA/BLA submissions, and quality systems experience, with leadership and
#J-18808-LjbffrGMP Quality Associate Director — Lead Clinical Batches in san francisco at Unknown Company
This position is listed as full time and onsite.