Validation Engineer developing documentation for commissioning and validation of pharmaceutical facilities in Italy. Requires travel in Italy and occasionally in Europe, with a focus on compliance and GMP.

Fundamentally we exist for one reason: To be the trusted solution for our clients as they strive to build a better working world and improve the human experience.
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Philosophically and practically, we believe that quality, cost, and schedule can be mutually reinforcing – trade-offs are not necessary.
Short-changing the focus on quality usually means problems down the road – problems that can cost money and delay the schedule.
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When your project requires planned, managed, and documented high quality to exacting global standards.
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When your project is complex, high-visibility, and carries significant risk.
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Validation Engineer developing documentation for commissioning and validation of pharmaceutical facilities in Italy. Requires travel in Italy and occasionally in Europe, with a focus on compliance and GMP.
Support sterililty assurance, contamination control and validation for sterile pharmaceutical manufacturing. Manage microbiological methods, protocols, client interactions and cross - functional projects.
Lead CAI's Quality, Compliance and Regulatory practice in Europe. Drive business development, client consulting, QMS implementation, and mentor consultants across European sites.
Lead sterility assurance, environmental qualification, and contamination control strategy. Execute aseptic process validation and sterilizing equipment qualification for pharmaceutical sterile products.