Description
The Medical Device Manufacturing Engineer develops and documents manufacturing processes, sets up and tests capital equipment, supports design and fixturing, assists with problem solving and test methods, and trains operators. The role requires at least three years of medical device development experience, including medical device capital equipment manufacturing, quality systems, and ISO 13485, along with a two-year technical degree or equivalent experience. Candidates must be able to work from both Bedford and Sudbury locations and travel between sites as needed.
