GMP IT/OT QA Specialist – System Validation Lead

03 ott - Ivrea
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Novartis in Ivrea, Italy is seeking a QA Specialist to support GMP-relevant IT/OT and computerized systems. The role focuses on qualification, validation, data integrity, and lifecycle documentation across manufacturing, QC labs, and utilities.
Responsibilities include reviewing validation deliverables, ensuring proper system ownership, and maintaining audits, deviations, and CAPAs to support compliant operations.
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