Qualification Specialist in Sterile Equipment Validation

15 ott - Lazio
BSP Pharmaceuticals

pBSP Pharmaceuticals S.p. A in Italy is seeking a Qualification Specialist to ensure rigorous documentation and validation activities for equipment and utilities in a high containment plant. /ppYou will lead analysis of technical documentation, draft and review DQ/IQ/OQ/PQ protocols, and generate qualification reports to meet GMP-compliant standards. The role emphasizes collaboration with purchasing for bid analyses and adherence to company procedures, with a focus on sterile environments. /p #J-18808-Ljbffr

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