Pharmacist | Pharmacist (m/w/d)

Job Summary

This role, situated within the Quality Control Team at a global Contract Research and Development Organization (CRDO), focuses on ensuring rigorous compliance across qualification and validation activities for innovative drug products, including biologics and cell therapies. The successful candidate will be responsible for compiling, reviewing, and approving critical documentation related to instrument qualification, equipment release for GMP use, and analytical method validation and verification. This involves defining validation strategies, managing the validation lifecycle, and ensuring traceability, acting as a key interface between GMP operations, QA, and IT. Key requirements include a Master’s degree in Pharmacy or a related scientific field, strong knowledge of GMP regulations, and at least three years of dedicated experience in equipment qualification and method validation within a regulated biopharmaceutical environment. This position offers the opportunity to contribute to improving human health by enabling drug development in a diverse, science-driven, and highly collaborative international setting near Munich.