Productlife Group is seeking a Validation Specialist to plan, coordinate, and execute Computerized System and software validation activities for client projects in regulated environments across GAMP 5, GMP, EU GMP Annex 11, and 21 CFR Part 11. You will draft validation documentation, manage risk assessments, and ensure data integrity per ALCOA+.
The role requires a 4–5 year track record, a Bachelor's or Master's in a relevant field, and fluent Italian and English, with travel as needed to
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📌 Gxp Csv Validation Specialist (Lazio)
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