You will be part of a collaborative cross-functional team, often consisting of members from Product Development Engineering, Clinical Affairs, Marketing, Regulatory Affairs, Production and Supplier Quality Engineering, Manufacturing Engineering, and Manufacturing, etc., to support new product development efforts, design changes, risk management activities, supplier changes, manufacturing and process changes, corrective and preventive actions (CAPAs), product complaint investigations, post-market surveillance, and other compliance projects, such as EU MDR uplift of existing products. Engineer, Design Quality is an active member of the Design Quality Engineering (DQE) team who will provide design assurance support for our existing commercially released medical devices, as well as new product development projects.