GMP Validation Engineer – Pharmaceutical Equipment

Aenova Group, at the Borgo San Michele LT site in Italy, is looking for an Engineering Validation Specialist to contribute to qualification activities for manufacturing equipment, process systems, utilities and laboratory instruments.

You will prepare GMP documentation (URS, DQ, IQ, OQ, PQ) and support FAT/SAT, collaborating with Engineering, Production, Quality Assurance, Validation, Maintenance, and suppliers. A degree in science/engineering and 2–3 years of experience are required.

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