CAI is a professional services company established in 1996, with nearly 800 employees worldwide. We serve the Life Sciences and Mission Critical industries, delivering critical solutions in high-stakes environments through rigorous processes, field-tested methods, and elite expertise developed over 30 years.
Our purpose is to be the trusted solution for our clients, helping build a better working world and improve the human experience. We are committed to our Foundational Principles: acting with integrity, serving each other and society, and working for our future.
At CAI, we pursue excellence, challenge industry standards, and operate at the intersection of wisdom, technology, and humanity. Operational readiness is a way of life for us, driven by effort, precision, and innovation. We focus on how things will be done, not how they used to be.
Key Responsibilities:
* Major Area 1: We are seeking a CQV Engineer for our operations in Italy. The role involves developing documentation for Commissioning, Qualifications, and Validation, including protocol writing, execution, and report development at client sites.
* Support documentation: Support documentation for commissioning, qualification, and validation of pharmaceutical facilities, utilities, and equipment.
* Protocol management: Responsible for protocol writing, execution (field verification), and report development at client sites.
* Position Requirements: BS or MS in a relevant science or engineering field, or equivalent experience; 4-8 years’ experience in commissioning/qualification in FDA-regulated industries; expertise in biotech, aseptic processing, gene therapy, etc.; proficiency in Microsoft Word and Excel; excellent English skills; willingness to travel in Italy and Europe.
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Additional competencies include strategic planning, customer focus, execution leadership, influencing others, talent development, results orientation, and leading safely and courageously.
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