Qualification Specialist in Sterile Equipment Validation

24 ott - Italia
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A in Italy is seeking a Qualification Specialist to ensure rigorous documentation and validation activities for equipment and utilities in a high containment plant. You will lead analysis of technical documentation, draft and review DQ/IQ/OQ/PQ protocols, and generate qualification reports to meet GMP-compliant standards. The role emphasizes collaboration with purchasing for bid analyses and adherence to company procedures, with a focus on sterile environments.

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