Hybrid in Warsaw, Indiana
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Today
Experience supporting medical device manufacturing Process Validations Specific experience with process characterization, equipment IQOQ, process OQ, and PQ Specific experience with Test method Validation and Gage RR Experience with root cause analysis and problem-solving for both technical and process issues Working knowledge of design control and cGMP requirements for medical device manufacturing per FDA QSR and ISO13485-2003Ability to lead and prioritize multiple medium-complexity project ass
Easy Apply
Contract, Third Party
30 - 35