Validation Engineer - Medical Device Quality & APQP Lead
Weiss-Aug
Weiss-Aug, a leader in precision manufacturing, seeks a disciplined Validation Engineer in Fairfield, NJ to drive IQ/OQ/PQ protocols, develop Master Validation Reports, and lead PPAP/Validation activities for new customer programs. You will ensure compliance with GMP, ISO13485, and 21 CFR 820, write SOPs and technical documentation, support APQP, DOE, FMEA, and manage change controls. A minimum of five years in a medical device quality role and a four-year engineering degree are required. #J-18808-Ljbffr Weiss-Aug
Vacancy posted 1 day ago
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