A leading engineering firm in Italy is seeking a Validation Engineer to support documentation for commissioning and validation of pharmaceutical facilities. The role involves developing protocols, managing the CQ documentation lifecycle, and providing cGMP guidance. Applicants should have a BS or MS in relevant fields and 3-5 years of experience, along with strong problem-solving skills and proficiency in Microsoft Office. Availability for travel throughout Italy is required.br#J-18808-Ljbffr