Design Quality Engineer II - Hardware (Surgical Robotics)

Medtronic

Closes in 6 days Hybrid

Quick summary

Work type
Hybrid
Location
North Haven, CT
Salary
$79,200–$118,800 / yr
Posted
2 days ago
Closes
Jun 26, 2026 (soon)

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $173k
This role $99k
$64k most similar roles pay here $225k

This role pays less than 98% of similar roles. Most pay $136,400–$209,750 — the shaded band above. At the midpoint, this role pays about $99k versus about $173k for comparable roles.

Based on 240 similar postings.

Employer

About Medtronic

Medtronic plc is the world's largest medical technology company by revenue, specializing in device-based therapies for over 70 health conditions.

Medtronic currently has 85 open roles on FindRole.

Listed pay typically runs $122,400–$183,600 across 84 roles with salary data.

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View all roles at Medtronic

At a glance

TL;DR · Design Quality Engineer II - Hardware (Surgical Robotics)

As a Design Quality Engineer II on Medtronic’s Surgical team in North Haven, Connecticut, you will play a pivotal role in ensuring the quality and safety of innovative surgical robotics systems. Your responsibilities include leading design quality and risk management activities such as DFMEA development and cross-functional reviews, maintaining the Product Risk Management File throughout the product lifecycle, and collaborating with R&D to embed quality controls into system requirements. You will also translate design requirements into robust manufacturing controls, support supplier qualification, and ensure serviceability and reliability considerations are incorporated into product design. This role requires expertise in hardware systems, electrical safety standards like IEC 60601, and experience working cross-functionally with manufacturing teams. Ideal candidates have a background in Electrical Engineering or Biomedical Engineering, along with hands-on experience in design risk management and statistical analysis tools.

What you'll do

  • Lead and support design quality and risk management activities, including DFMEA development.
  • Own and maintain elements of the Product Risk Management File throughout product lifecycle.
  • Translate design and CTQ requirements into robust manufacturing controls and inspection strategies.
  • Support supplier qualification and quality activities, ensuring design-related inputs are addressed.
  • Contribute to electrical safety and compliance activities, aligning risk identification with test strategy.

What we're looking for

  • Bachelor’s degree in Electrical Engineering, Biomedical Engineering, or related field.
  • 2+ years of experience in electrical engineering, quality engineering, or manufacturing quality roles.
  • Experience with capital equipment and complex electromechanical medical devices.
  • Familiarity with IEC 60601 or other electrical safety standards.
  • Hands-on experience with design risk management, including DFMEA development.
  • Ability to collaborate cross-functionally with R&D, manufacturing, and suppliers.
  • Knowledge of statistical analysis tools for quality testing and root cause investigations.

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Hybrid