CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Life Sciences and Mission Critical industries that need to deliver critical solutions in high‑stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest standard through our rigorous approach, field‑tested processes, and elite expertise developed over 30 years.
We exist to be the trusted solution for our clients as they strive to build a better working world and improve the human experience.
We serve each other
We serve society
From the beginning, we’ve challenged ourselves to do what others wouldn’t. We operate at the intersection of wisdom and technology and thrive when they come together with humanity. For us, operational readiness isn’t simply a goal. We do this through tireless effort, precision, efficiency and an unwavering belief that there is always room for advancement. 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.
BS or MS in a relevant science or engineering field, or equivalent years of hands‑on experience.
Minimum 2‑3 years’ experience performing commissioning and/or qualification activities in an FDA regulated industry. Ideally, experience in facilities and equipment startup, walk‑downs & troubleshooting, utilities (WFI, RO, HVAC), building automation or other pharmaceutical manufacturing processes and equipment, FAT/SAT, URS, design review, P&IDs;, IQ/OQ/PQs, generation & execution, etc.
Provide cGMP leadership and guidance for the integration and delivery of CQV services for our Life Sciences clients.
Excellent technical problem‑solving and troubleshooting skills, with solid knowledge of typical project technical issues.
Ability to work independently while quickly building an
📌 Test ingenieur (Italia)
🏢 Cai
📍 Italia