The product engineering II supports sustaining engineering activities for stapling products in the Released Product Engineering (RPE) group within the CSI. This role is responsible for evaluating and implementing product and process changes, developing design and test documentation, supporting investigations, and collaborating across functions to resolve product, supplier, and manufacturing issues while maintaining compliance with medical device regulations and design control requirements.Within the RPE group, this role focuses on sustaining engineering for commercially released products, including Open, Laparoscopic stapling devices and GYN products. The team partners closely with Manufacturing, Quality, Regulatory Affairs, and suppliers to maintain product performance, quality, compliance, and continuity of supply throughout the product lifecycle. This position is based in North Haven, CT and follows a hybrid work model requiring on-site presence four days per week. Travel is expected to be minimal and may include visits to manufacturing sites or suppliers as needed.
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Job Type
Full-time
Career Level
Entry Level