GMP IT/OT QA Specialist — Systems Validation
Pubblicato il 16-10-2026 - Novartis in Italia
Novartis Ivrea is seeking a QA Specialist to provide QA oversight for GMP-relevant IT/OT and computerized systems during ramp-up, focusing on system qualification, validation, data integrity, and lifecycle documentation.
You will ensure compliant operation of IT/OT systems in manufacturing and labs, support audits and inspections, collaborate across IT, OT, Quality, and operations, and help establish local quality capability for IT/OT qualification and initial manufacturing-line validation.
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