CQV Engineer: Pharma Facility Validation Lead

NTT DATA Europe & Latam is seeking an experienced professional for the Commissioning, Qualification, and Validation (CQV) of pharmaceutical facilities in Italy. The ideal candidate will have 4–8 years of relevant experience in FDA-regulated industries, ensuring compliance and timely completion of all documentation. Responsibilities include supporting execution and management of CQV documentation and providing cGMP leadership. Availability for travel throughout Italy and occasional European travel is required.
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