CQV Engineer — Life Sciences Validation Specialist

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7cd0c6

CAI is seeking a CQV specialist to support documentation for commissioning, qualification, and validation of pharmaceutical facilities and equipment. You will write protocols, conduct field verifications, and develop summary reports at client sites in a fast-paced Life Sciences environment.
The role requires 2–3 years of FDA-regulated CQV experience, strong problem-solving skills, and the ability to travel within Italy and abroad. A BS or MS in a relevant field is preferred.
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Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7cd0c6