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Senior Director of QA — Clinical GxP & Compliance

Fortvita Biologics, Palo Alto, California, United States, 94306

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A biotechnology firm in Palo Alto is seeking a Director of Quality Assurance to lead quality assurance activities across clinical development. The role involves overseeing compliance with Good Clinical Practice (GCP), developing Quality Assurance programs, and serving as the primary QA liaison. Candidates should possess a BS/BA in a relevant scientific discipline and a minimum of ten years of experience in the QA function within the pharmaceutical industry. This is an onsite role offering a collaborative work environment. #J-18808-Ljbffr