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BSP Pharmaceuticals S.p. A is expanding its quality and data integrity team to strengthen validation of computerized systems in lab and production environments. The CSV & Data Integrity role focuses on validation planning, IQ/OQ/PQ execution, system configuration, documentation, and collaboration on SOPs and the Validation Master Plan. A Master’s degree and experience with 21 CFR Part 11 are required. #J-18808-Ljbffr
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AM International