Specific activities and responsibilities: - Execution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment - Preparation of validation protocols, reports and related documentation. - knowledge of GMP regulations - Ensure compliance with
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
Specific activities and responsibilities: Execution, and documentation of calibration and qualification activities (IQ/OQ/PQ) for facilities, utilities and equipment Preparation of validation protocols, reports and related documentation. knowledge of GMP regulations Ensure compliance with GMP requirements and internal
About Us ProductLife Group (PLG) is a dedicated life sciences and pharmaceutical outsourcing and consulting company providing expertise and services in areas such as: Product Development, Market & Patient Access, Regulatory Affairs and Safety & Vigilance
ProductLife Group is seeking a Validation Specialist Associate to join PLG Center of Expertise Engineering around Mirandola, Italy, with a hybrid work policy. You will own qualification and validation activities for facilities, utilities and equipment, and contribute to GMP-compliant
Teoresi S.p.A. , 35+ anni di storia , 8 società tra Italia, Stati Uniti, Germania, Svizzera, +1200 risorse , 4 acquisizioni in un anno, 1 solo partner ed un’unica soluzione. Potrebbe essere proprio lei il candidato/la
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