CSV & Data Integrity Specialist
BSP Pharmaceuticals S.p.A. in Italy seeks a specialist for the CSV & Data Integrity area to advance validation activities of laboratory and production computer systems.
You will draft validation documents, execute IQ/OQ/PQ protocols, maintain traceability matrices, review vendor documents, and contribute to SOPs and the Validation Master Plan in a highly regulated CDMO environment.
Experience with 21 CFR Part 11 and data integrity principles is essential.
You will draft validation documents, execute IQ/OQ/PQ protocols, maintain traceability matrices, review vendor documents, and contribute to SOPs and the Validation Master Plan in a highly regulated CDMO environment.
Experience with 21 CFR Part 11 and data integrity principles is essential.