Description
Acadia Pharmaceuticals is hiring a Sr. Manager, Quality Control EU to lead analytical methods, specifications, validations, transfers, release testing, stability programs, and regulatory-quality documentation for drug substances and drug products outside North America. The role manages contract service providers, coordinates stability studies, reviews analytical data and reports, supports inspections and regulatory filings, and leads OOS, OOT, and CAPA investigations. A bachelor’s degree in a health science discipline is required, with a master’s degree preferred, along with 3–5 years of pharmaceutical manufacturing quality control or quality assurance experience and knowledge of EU, Japanese, and FDA GMP and ICH requirements.
