Qa/Qc Specialist: Gmp Validation & Deviation Management
BSP Pharmaceuticals S.P.A.Si candidi ora: legga i dettagli del lavoro scorrendo verso il basso. Verifichi di possedere le competenze necessarie prima di inviare la candidatura.is a CDMO offering development and manufacturing services for cytotoxic and non-cytotoxic therapies.The role supports deviation investigations, CAPA implementation, validation activities, and audit readiness within a regulated environment. xysqume Responsibilities include preparing validation protocols and reports, collaborating with cross-functional teams, and ensuring compliance with SOPs and regulatory standards during manufacturing and cleaning validations.#J-18808-Ljbffr