pCAI 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.
/ppRequired 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.
/p #J-*****-Ljbffr
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