Associate Director, GVP Audit & R&D Quality

A leading biopharmaceutical company is seeking an Associate Director for Good Pharmacovigilance Practice Audits in California. This position involves overseeing GVP audits, supporting regulatory inspections, and enhancing quality processes. The ideal candidate will have significant experience in quality compliance within the biopharma sector, alongside strong leadership and strategic thinking skills. This role is integral to maintaining high standards in audit practices and regulatory compliance. #J-18808-Ljbffr