What to Expect Work 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. Qualifications 2-3 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 All applications will be managed by the Swiss partner, fully respecting Swiss legal requirements. Tagged as: cqv engineer #J-18808-Ljbffr Resourcing Life Science
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