CAI is seeking a CQV Engineer to join our Italian operations. The role develops documentation to support Commissioning, Qualifications, and Validation, including protocol writing, field verification, and summary reports at client sites.
Required are 4–8 years of FDA-regulated CQV experience, knowledge of GMP processes, and strong English. Expect travel in Italy and abroad, with compensation €45,000–€57,000 gross per year.
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