Quality Engineer II- Manufacturing Operations

Quality Engineer II
- Manufacturing Operations Skip to main content

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- Manufacturing Operations page is loaded## Quality Engineer II
- Manufacturing Operations Apply remote type:
Onsite locations:
Irvine, California, United States of America time type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
June 27, 2026 (10 days left to apply) job requisition :
R69707

We anticipate the application window for this opening will close on - 27 Jun 2026

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 onsite 5 days a 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.
The Medtronic Global Operations and Supply Chain (GOSC) organization is seeking a Quality Engineer II to join our growing Quality Operations team in Irvine, California. In this role, you will support key programs within our Quality Management System and help drive day-to-day quality and compliance activities in the development and manufacturing of innovative medical devices.
We are looking for a collaborative, hands-on professional who is motivated to make an impact in a dynamic environment. The ideal candidate brings strong analytical skills, a solid foundation in quality engineering principles, and the ability to manage multiple priorities effectively while continuing to grow professionally.
Please note that this is a fully onsite role based in Irvine, California.

** Responsibilities may include the following. Additional duties may be assigned as needed.
*** Develop, modify, apply, and maintain quality standards and protocols for processing materials into partially finished or finished products.
* Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
* Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
* Design or specify inspection and testing methods and equipment, conduct quality assurance testing, and perform statistical analyses to evaluate product or material nonconformance and support resolution.
* Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
* Contribute expertise in areas such as design quality, incoming materials, production control, product evaluation and reliability, inventory control, and research and development as they relate to product or process quality.
** Must Have:

Minimum Requirements
** Requires a Baccalaureate degree and minimum of 2 years of relevant Quality experience OR Master's degree with a minimum of 0 years relevant experience.
** Nice to Have
*** Bachelor’s degree required in Mechanical Engineering (preferred), Industrial Engineering, Biomedical Engineering, or a related field.
* Knowledge of statistical tools such as ANOVA, capability analysis, and DOE.
* Ability to collaborate effectively with cross-functional teams.
* Experience with NCMRs, CAPAs etc.
* DRM or Design for Six Sigma certification.
* Experience with process validation.
* Experience with test method validation.
* Experience in medical device manufacturing and familiarity with…