Qa/Qc Specialist: Gmp Validation

Pubblicato il 11-11-2026 · BSP Pharmaceuticals · Baia - Latina

BSP Pharmaceuticals S.p. A.
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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.
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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.
Max. 8 MB. Formati Accettati: PDF, RTF, DOC, DOCX, ODT.