GMP Validation Associate & Documentation Specialist

22 set - Emilia-Romagna
Productlife Group

ProductLife Group is seeking a Validation Specialist with 1-2 years of experience to execute calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment. The role includes drafting validation documentation and SOPs, ensuring GMP compliance.

The candidate will collaborate with QA, Production, Engineering and QC teams, maintain validated states of equipment and processes, and be comfortable traveling to client sites. Proficiency in English and Italian required.

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