Responsibilities Verifichi qui sotto se possiede i requisiti per questa occasione e, in tal caso, invii la sua candidatura il prima possibile. Develops documentation to support Commissioning, Qualifications, and Validation Responsible for protocol writing and execution, field verification, and development of summary reports at client sites Provide cGMP leadership and guidance for the integration and delivery of CQV services for Life Sciences clients Support onsite and offsite activities such as FATs, SATs, IOQ, and PQ Executions and System Walkdowns Requirements BS or MS in a relevant science or engineering field,



or equivalent hands‐on experience Minimum 4-8 years' experience performing commissioning and/or qualification activities in an FDA regulated industry Experience in facilities and equipment startup, walk‐downs & troubleshooting, utilities (WFI, RO, HVAC), building automation or other pharmaceutical manufacturing processes and equipment, FAT/SAT, URS, design xrdztoy review, P&IDs;, IQ/OQ/PQs, generation & execution Excellent technical problem‐solving and troubleshooting skills Familiarity with Baseline Guide 5 (Second Edition) a plus Expertise in Microsoft Word and Excel Excellent oral and written English #J-18808-Ljbffr

📌 Staff II CQV Engineer (Italia)
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📍 Italia