About this role
Associate Director, Quality Validation at Revolution Medicines. Location: Redwood City, California, United States. Role: providing oversight, leading validation, ensuring compliance Requirements: Bachelor's in a scientific/engineering/technical discipline; 10+ years GMP quality experience with validation (PPQ, CPV, cleaning, packaging, transportation); experience with CMOs, regulatory inspections, and risk-based decision making. Category: Quality Assurance Seniority: Senior Level Tools: electronic quality systems, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, Microsoft Visio Commitment: Full Time Workplace: Hybrid Languages: English