Medical Device Process Engineer - DHF & Validation Lead
Viltis
Viltis is seeking a Process Engineer to support a DHF remediation initiative in a regulated medical device manufacturing environment in Richmond, Illinois. This on-site contract role emphasizes design controls, process validation, risk management, and technical documentation. You will lead cross-functional activities with engineering, quality, manufacturing, and operations, author DHF documentation, own IQ/OQ/PQ, develop PFMEA, and apply DOE and statistical methods to guide decisions while #J-18808-Ljbffr Viltis
Vacancy posted 3 days ago
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