CQV / Commissioning Qualification Validation Engineer – Italy

5 giorni fa


Rome, Italia Resourcing Life Science A tempo pieno

What to ExpectWork closely with engineering teams to plan and execute commissioning activities. Create detailed commissioning plans, protocols, and reports for production equipment and room qualifications. Conduct thorough checks to ensure equipment and systems are fully functional. Quickly identify and resolve issues that arise during commissioning. Develop qualification protocols and comprehensive test plans for equipment, systems, and processes. Perform Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). Maintain meticulous documentation of qualification tests and analyze results. Identify and correct any deviations from established specifications. Work with cross-functional teams to resolve validation discrepancies. Create and implement validation protocols for processes and systems, ensuring compliance with industry standards.Qualifications2-3 years of technical experience as a CQV Strong knowledge of industry regulations (FDA, GMP, GAMP). Excellent troubleshooting and problem‑solving skills. Very good English language skills, both written and spoken#J-18808-Ljbffr



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    What to ExpectWork closely with engineering teams to plan and execute commissioning activities.Create detailed commissioning plans, protocols, and reports for production equipment and room qualifications.Conduct thorough checks to ensure equipment and systems are fully functional.Quickly identify and resolve issues that arise during commissioning.Develop...


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    A life sciences company in Italy is seeking a skilled CQV professional to plan and execute commissioning activities. The ideal candidate should have 2-3 years of technical experience, strong knowledge of FDA, GMP, and GAMP regulations, and excellent troubleshooting skills. Responsibilities include developing qualification protocols and maintaining detailed...

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