Quality Engineer, Medical Devices - Sterile & Risk

A leading medical device company in Massachusetts is seeking a Quality Engineer to oversee compliance in the development of sterile, single-use medical devices. Responsibilities include supporting risk management activities, conducting compliance testing, and collaborating with cross-functional teams. The ideal candidate will possess a Bachelor's degree in Engineering or Life Sciences and have 5–7 years of relevant experience, alongside strong communication and statistical analysis skills.

This role promises opportunities to impact product quality and compliance substantially.
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