QA & Validation Specialist - GMP Compliance & Audits

BSP Pharmaceuticals S.p.A. is seeking a QAC Specialist to ensure quality during manufacturing of high-potency anticancer drugs. You will investigate process deviations, propose CAPAs, validate processes and support client/regulatory audits in a GMP environment.The role requires a scientific degree, GMP knowledge, and proven QA experience in multinational...

BSP Pharmaceuticals S.p.A. 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.Responsibilities include preparing validation protocols and reports, collaborating with...

BSP Pharmaceuticals S.p.A. 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.Responsibilities include preparing validation protocols and reports, collaborating with...

Per una società di consulenza specializzata nei servizi tecnici e di compliance per l'industria farmaceutica , ricerchiamo un Validation Specialist da inserire nella sede di Latina . La risorsa entrerà a far parte di un team dedicato a progetti di consulenza sviluppati per importanti realtà del settore farmaceutico, operando a stretto contatto con i...

Per una società di consulenza specializzata nei servizi tecnici e di compliance per l'industria farmaceutica , ricerchiamo un Validation Specialist da inserire nella sede di Latina . La risorsa entrerà a far parte di un team dedicato a progetti di consulenza sviluppati per importanti realtà del settore farmaceutico, operando a stretto contatto con i...

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across...

CSV Life Science Group is seeking a Validation Specialist to join its CQV team in Milan and Latina offices. The resource will draft and execute qualification protocols (DQ/IQ/OQ/PQ) for equipment, facilities and controlled environments, ensuring compliance with EU GMP and related standards. The role includes thermal mapping, instrument calibration, and...

BSP Pharmaceuticals S.p.A. is seeking a QAC Specialist to ensure quality during manufacturing of high-potency anticancer drugs. You will investigate process deviations, propose CAPAs, validate processes and support client/regulatory audits in a GMP environment. The role requires a scientific degree, GMP knowledge, and proven QA experience in multinational...

BSP Pharmaceuticals S.p.A. 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. Responsibilities include preparing validation protocols and reports, collaborating with...