Job Description
📋 Description Define regulatory standards for AI-driven drug discovery. Stand up clinical quality systems and QMS processes. Lead global vendor audits for CROs/CMO/CDMOs. Partner with Compute and Data Science on AI/ML validation. Hybrid, in-person role based in South San Francisco. 🎯 Requirements 10+ years of QA in biotech/pharma. GXP mastery: GLP, GCP, GMP. Extensive vendor audits and regulatory inspections. Tech literacy: Computer System Validation. Hands-on SOP writer and documentation expert. Cross-functional collaboration with scientists and engineers. 🎁 Benefits 401(k) with employer matching. Comprehensive medical, dental, and vision coverage. Open, flexible vacation policy. Paid parental leave (16 weeks for birth, 10 for new parent). Stipends for home office, cell phone, and internet. Support for conferences, books, and professional development.
