Medtronic

Design Quality Engineer II - Hardware (Surgical Robotics)

Medtronic$79K — $118K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Electrical or Biomedical Engineering or related technical field
  • 2+ years of relevant work experience; or a Master's with 0-2 years
  • Experience with capital equipment or complex electromechanical devices
  • Background in a regulated industry, preferably medical devices
  • Familiarity with IEC 60601 or electrical safety standards

Responsibilities

  • Lead design quality and risk management activities including DFMEA
  • Maintain elements of the Product Risk Management File throughout the lifecycle
  • Embed quality and risk controls into system and design requirements with R&D
  • Translate design and CTQ requirements into manufacturing controls
  • Support design transfer, production readiness, and issue resolution with manufacturing teams
  • Assist in supplier qualification and quality activities with design inputs
  • Ensure serviceability and reliability considerations are incorporated into product design

Benefits

  • Health, dental, and vision insurance
  • Health Savings Account and Flexible Spending Account
  • Life and long-term disability insurance
  • Tuition assistance/reimbursement
  • Incentive plans and 401(k) with employer match
Full Job Description
We anticipate the application window for this opening will close on - 17 Jul 2026

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 components
    2-5 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 surveillance, complaints, and/or CAPAs
  • Familiarity with statistical analysis tools (e.g., Minitab, JMP)
  • Prior exposure to manufacturing or operations environments
  • Exposure to serviceability, field support, or equipment maintenance considerations in product design
  • Ability to work independently, manage priorities, and influence without direct authority
  • Strong written and verbal communication skills

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. a7 214.2(h)(4)(iii)(A) is required.

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

U.S. Work Authorization & Sponsorship

At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.

Recruitment Fraud Alert

We are aware of phishing scams targeting job seekers. Please keep the following in mind:

Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official [redacted].com email addresses.

Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.

If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.

If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at [redacted].

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

Salary ranges for U.S (excl. PR) locations (USD):$79,200.00 - $118,800.00

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

About Medtronic

Medtronic plc is an Irish-domiciled multinational medical device company that develops and manufactures medical device technologies and therapies to treat chronic diseases worldwide. Medtronic was founded in 1949 in Minneapolis, Minnesota, as a medical equipment repair shop. Today, the company operates in more than 160 countries and employs over 90,000 people. Medtronic's primary products include implantable pacemakers and defibrillators, insulin pumps, spinal and neurostimulation devices, surgical tools, and patient monitoring systems. The company is committed to improving patient outcomes and expanding access to healthcare through innovative medical technologies.
Learn more about Medtronic
Size
95,000 employees
Market Cap
$102.7 billion
Industry
Net Income
$2.8 billion
Founded
1949
5 Year Trend
+1.3%
Revenue
$27.9 billion
NASDAQ

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