CQV Validation Specialist — GMP, IQ/OQ/PQ & Documentation

05 ago - Bologna
Altro

ProductLife Group is seeking a validation specialist in Italy (Emilia-Romagna) to execute calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment. You will prepare validation protocols and reports, ensuring GMP compliance and maintaining validation documentation.
The role requires 3-4 years of experience, a Bachelor's degree in a related field, and professional fluency in English and Italian.

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