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Design Quality Engineer II - Hardware; Surgical Robotics

Job in North Haven, New Haven County, Connecticut, 06473, USA
Listing for: Medtronic Plc
Full Time position
Listed on 2026-06-27
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer, Biomedical Engineer, Electronics Engineer
Job Description & How to Apply Below
Position: Design Quality Engineer II - Hardware (Surgical Robotics)

Design Quality Engineer II

At Medtronic, you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We're working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. This position is onsite 4 days per week in North Haven, Connecticut.

Our Medtronic Surgical team is working to bring the benefits of minimally invasive surgery (MIS) to more people and places through a portfolio of robotic and digital solutions. Together, we are working to broaden options and expand access globally for hospitals, surgeons, and patients.

As a Design Quality Engineer II, you will play a critical role supporting the design quality, risk management, and U.S. launch of innovative surgical robotics systems, capital equipment, and instrumentation, including the Hugo™ platform.

This design-focused quality role works at the intersection of R&D, manufacturing, supplier quality, and regulatory, supporting medical device designs from early development through manufacturing transfer and post-launch support.

You will translate design and risk requirements into effective manufacturing controls, ensuring quality is built into the product from the outset, with a specific focus on hardware systems, electrical safety, and capital equipment performance in the field, while operating with a high degree of autonomy and cross-functional influence.

Key Responsibilities
  • Lead and support design quality and risk management activities, including DFMEA development and cross-functional risk reviews
  • Own and maintain elements of the Product Risk Management File throughout the product lifecycle
  • Partner with R&D to embed quality and risk controls into system, hardware, and design requirements
  • Translate design and CTQ requirements into robust manufacturing controls and inspection strategies, including hardware performance and safety requirements
  • Collaborate with manufacturing teams to support design transfer, production readiness, and issue resolution
  • Support supplier qualification and supplier quality activities, including design-related inputs
  • Support design quality activities for capital equipment and electromechanical systems, including hardware integration and system-level considerations
  • Contribute to electrical safety and compliance activities (e.g., IEC 60601), including risk identification and test strategy alignment
  • Partner with cross-functional teams to ensure serviceability, reliability, and field maintenance considerations are incorporated into product design
  • Perform quality testing, statistical analysis, and root-cause investigations to address nonconformances and CAPAs
  • Participate in design reviews, change management, and technical decision-making
  • Support complaint investigations, post-market activities, and U.S. launch hyper-care efforts
Required Qualifications
  • Bachelor's degree in Electrical Engineering, Biomedical Engineering, or a related hardware-focused technical discipline, plus:
    2+ years of related work experience OR a Master's degree with 0–2 years of related work experience
Preferred Qualifications
  • Experience working with capital equipment or complex electromechanical medical devices
  • Familiarity with IEC 60601 or other electrical safety standards
  • Experience with hardware systems, PCBAs, or electromechanical components2–5 years of experience in Electrical Engineering, Quality Engineering, Design Quality, Manufacturing Quality, or related roles
  • Background in a regulated industry (medical devices strongly preferred; robotics, capital equipment, or aerospace highly relevant)
  • Hands-on experience with design risk management, including DFMEA
  • Experience working cross-functionally with manufacturing teams and suppliers
  • Experience supporting U.S. product launches, post-market…
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