CQV Engineer – Life Sciences Validation

13 ago - Milano
Cagents

Cagents seeks a CQV Engineer to join our expanding Italy operations. You will develop documentation for Commissioning, Qualification, and Validation, write and execute protocols, perform field verifications, and craft summary reports at client sites.
Requirements include a BS/MS in science or engineering, 2–3 years in commissioning/qualification in FDA-regulated environments, strong MS Word/Excel skills, cGMP leadership, and willingness to travel in Italy and abroad.

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