Consultant, Medical Devices, Design Quality Engineer - (Warsaw, IN)

Consultant, Medical Devices, Design Quality Engineer, Subject Matter Expert Summary Our client, a growing medical device manufacturer, has engaged GForce Life Sciences to identify a design quality engineer to assist in New Product Introduction (NPI) and to assure that our clients products, processes, procedures, and systems continue to comply with regulatory qualifications as they are submitted for approval to regulatory bodies. Duties / Expectations of Role Responsible for assuring products conform to established qualifications and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, Formulates procedures, specifications, and standards such as: Review/approve prints Review/ inputs to design inputs, outputs