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Principal Quality Engineer

LocationMounds View, Minnesota, United States of America
PayNot listed
Work arrangementNot specified
Job typeFull-time
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ApplicationContinue to employer career siteYou’ll complete your application on Medtronic’s hiring system.
Last checked27 days ago

About the role

We anticipate the application window for this opening will close on - 9 Oct 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life At Medtronic, we push the limits of what technology can do to make tomorrow better than yesterday and that makes it an exciting and rewarding place to work. We value what makes you unique. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations. The Cardiac Surgery Operating Unit develops and delivers innovative surgical solutions that enable surgeons to treat complex heart conditions, including coronary artery disease, structural heart disease, and cardiopulmonary support needs. In this exciting role as a Principal Quality Engineer supporting the Post Market Quality organization, you will provide technical leadership across all quality aspects of the commercial portfolio, including Health Risk Assessments, Post Market Surveillance, and Risk Management. You will serve as a key partner to cross functional teams, guiding critical quality decisions that protect patients and ensure sustained product performance. 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 are working onsite a minimum of 4 days per week 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 role will require less than 10% of travel to enhance collaboration and ensure successful completion of projects. Responsibilities may include the following and other duties may be assigned:

  • Risk Management: Support risk assessments and hazard analyses based on post-market data. Lead Health Risk Assessments to determine potential risk and recommend need for Field Corrective Action (FCA).
  • Post-Market Surveillance: Monitor product performance in the field, collect and analyze reliability data, and identify trends and potential issues.
  • Root Cause Investigation and Failure Analysis: Lead investigations into product failures and complaints, utilizing root cause analysis techniques to determine underlying causes. Support complaint trending and investigations of complaint trend excursions or quality signals from the field.
  • Design Control: Assess design and risk impacts of changes; generate, review, and approve FMEAs, test method validations, and verification and validation test reports in compliance with medical device design control requirements.
  • Continuous Improvement: Collaborate with design, manufacturing, and quality teams to implement design, process or supplier changes, corrective and preventive actions that enhance product reliability.
  • Customer Interaction: Provide technical support to customers and field personnel regarding reliability issues and product performance.
  • Coaching: Provide technical mentorship and coaching to junior engineers.

Preferred qualifications

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Preferred qualifications

  • Prior experience in the medical device industry across product development, operations, or quality functions.
  • Demonstrated expertise in risk management in accordance with ISO 14971.
  • Strong technical writing and communication skills, with the ability to clearly explain complex technical topics to non-technical audiences.
  • Proven ability to lead root cause investigations, solve complex technical problems, and perform statistical data analysis. Must Haves: Required

What they're looking for

  • Requires a Baccalaureate degree in Science, Technology, Engineering, Math or a related technical discipline with a minimum of 7 years of relevant experience OR
  • Master's degree with a minimum of 5 years relevant experience OR

Benefits

‌ Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values.

Equal opportunity

equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law.

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Principal Quality EngineerMounds View, Minnesota, United States of America