QA/QC Specialist: GMP Validation & Deviation Management
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 cross-functional teams, and ensuring compliance with SOPs and regulatory standards during manufacturing and cleaning validations.
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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.
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