Senior Medical Device Quality Engineer – Hybrid, Impact

GSK US is seeking a Quality Engineer for medical device products across design, manufacturing, and regulatory teams. You will ensure product safety, reliability, and compliance while leveraging data-driven problem solving and cross-functional collaboration to improve patient outcomes.

This hybrid role requires a bachelor's in engineering or quality, 5+ years in medical device quality engineering or regulated manufacturing, knowledge of ISO 13485 and FDA 21 CFR part 820, and experience with

This opportunity is for the Senior Medical Device Quality Engineer – Hybrid, High Impact role at Regulatory Toolkit.

This role is for the Senior Medical Device Quality Engineer – Hybrid, High Impact role at Regulatory Toolkit.

We are seeking a motivated Senior Medical Device Quality Engineer – Hybrid, High Impact to join Regulatory Toolkit in Lower Providence Township, PA, United States.