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BSP Pharmaceuticals S.p.A. is expanding its CSV & Data Integrity team to validate laboratory and production computer systems, including analytical instrumentation, HMI, and SCADA.
The role focuses on drafting validation documents, planning, and execution of IQ/OQ/PQ, with strong emphasis on compliance with 21 CFR Part 11 and data integrity principles. The ideal candidate holds a Master's degree in a scientific discipline and has experience in GMP environments, ready to contribute to the
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