CONMED is seeking a Design Quality Engineer to support quality activities across the medical device lifecycle, from concept to commercialization and sustaining. You will be the quality engineering contact on cross‑functional teams to ensure compliance with QSR, ISO 13485, EU MDR, and related standards. The role emphasizes risk management, design verification and validation, and CAPA leadership, with collaboration across manufacturing and suppliers to ensure product safety, reliability, and

Also on the board Same function, level within a rung

Level

Manager

Location

Greenwood Village, CO

Occupation

Validation Engineers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

4 days ago

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