Director, Quality Assurance - Technical

Role: Director, Quality Assurance - Technical, overseeing GMP compliance, validation, and technical quality for contract manufacturing, testing, and storage of drug substances and products up to Phase 3 validation and commercialization. Responsibilities lead validation efforts (process, facilities, equipment, computer systems) manage and support CSP oversight review validation plans and protocols handle change controls, deviations, investigations, risk management vendor qualification collaborate with Technical Operations Requirements Bachelor's in life sciences (Chemistry, Biology, Chemical Engineering preferred) 10+ years in FDA-regulated pharma/biotech industry deep knowledge of cGMPs and validation Preferred Master's degree experience with small molecule pharma strong project management cross-functional collaboration and leadership skills High-Value GMP validation contract manufacturing oversight validation of processes/equipment/cleaning/test methods experience with pharma regulations international travel (10-25%) remote work from San Diego Work setup primarily remote with some travel #J-18808-Ljbffr Scorpion Therapeutics