Role overview
Job description
Position Description: We are now seeking a CQV Engineer to join our growing operations in Italy. The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and execution, field verification, and development of summary reports at the client site. The role of a CQV Engineer in CAI is to: Support documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment. Responsible for protocol writing and execution (field verification), and development of summary reports at client sites. Position Requirements: High attention to detail Ability to multi-task and take initiative to accomplish assigned tasks accurately by established BS or MS in a relevant science or engineering field, or equivalent years of hands-on experience Minimum 4 – 8 years’ exper
…About this listing
- Source: CAI's official careers site (via Lever) · last confirmed on the source 1 Nov 2026
- Posted 30 Oct 2024
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What they are looking for
Skills & requirements
Qualification
The role of a CQV Engineer in CAI is to: Support documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment; Position Requirements: High attention to detail Ability to multi-task and take initiative to accomplish assigned tasks accurately by established BS or MS in a relevant science or engineering field, or equivalent years of hands-on experience Minimum 4 – 8 years’ experience performing commissioning and / or qualification activities in an FDA regulated industry; Familiarity with Baseline Guide 5 (Second Edition) a plus Expected skills: Isolators qualification protocols execution and reporting, VHP cycle development, GMP based knowledge Expertise in Microsoft Word and Excel Excellent oral and written English are required
Department · Europe Life Sciences
Hiring company
CAI
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