11 ago - Roma
Biotecnologie - Farmacia - Chimica
Groupe ProductLife is seeking a Validation Specialist (Data & Compliance) to lead CSV activities on client projects in Rome, Italy. You will ensure compliance with GAMP 5, GMP, EU GMP Annex 11 and 21 CFR Part 11, drafting validation documentation and supporting data integrity across projects.
The role requires 4–5 years of experience, a relevant engineering or life sciences degree, and fluency in Italian and English. Onsite work with travel to client sites as needed is expected.
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