13 ott
|
BSP Pharmaceuticals
|
Latina
13 ott
BSP Pharmaceuticals
Latina
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.
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📌 QA/QC Specialist: GMP Validation & Deviation Management (Latina)
🏢 BSP Pharmaceuticals
📍 Latina