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Manufacturing Validation Engineer (Medical Devices)
Ref No.: 18-52854
Location: Irvine, California
Position Type:Full Time/Contract
Start Date: 07/25/2018
Hands on Exp. on: Working knowledge of cGMP guidelines, FDA 21 CFR Part 820/210/211, ICH guidelines Writing IQ, OQ, PQ protocol and report for manufacturing equipment Engineering change order Development of a Standard Procedure (SP), related Work Instructions (WI), Forms, Checklists, Protocols, Reports & Templates for facilities/utilities, warehouse commissioning and qualification activity Writing IQ, OQ and PQ protocol and report of computer system validation