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Senior Quality Engineer - Warsaw, IN

Medtronic
United Statesfull_timeVerifiedPosted 7 Jul 2026
💰 $147,600/yr($98,400/yr$147,600/yr)

About the role

We anticipate the application window for this opening will close on - 14 Jul 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

         

         

Act boldly. Compete to win. Move with speed and decisiveness. Foster belonging. Deliver results…the right way. That’s the Medtronic Mindset — our cultural norms. Our brand is rooted in action, not just words. The Medtronic Mindset defines the expectations of our culture. Every person here plays a role in bringing it to life. We recognize your extraordinary potential to ensure future generations live better, healthier lives.

Medtronic – Warsaw, IN manufactures spinal implants and Brain/ENT instrument components. In this exciting and fulfilling role the Quality Engineer will be responsible for providing quality support to the product value stream, ensuring that customer and patient needs are met every day. They will be part of a passionate team dedicated to ensuring our products meet the highest standards.

The Senior Quality Engineer role is critical in supporting key department metrics and NPI (New Product Introduction) projects, contributing to the global strategy while delivering on our mission to manufacture products of the highest quality that alleviate pain, restore health, and extend the life of our patients. This is more than just a job. It is your chance to make a significant impact on someone’s life and to join a mission-driven organization that values growth and development.

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 5 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. 


Responsibilities may include the following and other duties may be assigned.

  • Develop, modify, apply and maintain quality standards and protocol for processing materials into partially finished or finished materials product.

  • Collaborate with engineering and manufacturing functions to ensure quality standards are in place.

  • Devise and implement methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.

  • Perform NCMR investigation and disposition.

  • Contribute to continuous improvement projects.

  • Design or specify inspection and testing mechanisms and equipment; conduct quality assurance tests; and perform statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.

  • Ensure that corrective measures meet acceptable reliability standards, and that documentation is compliant with requirements.

  • May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and/or research and development as they apply to product or process quality.

Must Have: Minimum Requirements

  • Bachelor’s Degree in Engineering, Science or Technical field with 4+ years of work experience in Engineering and/or Quality OR Advanced Degree in Engineering, Science or technical field with 2+ years of work experience in Engineering and/or Quality OR PhD with 0 years of relevant experience

Nice to Have

  • NPI (New Product Introductions) experience

  • Requires 3-D Printing/Additive Manufacturing experience

  • Experience working in a fast-paced manufacturing environment

  • Experience developing, executing and analysis of Test Method Validations

  • Ability to build and maintain positive relationships with others

  • Ability to multi-task and to take initiative

  • Strong critical thinking and analytical skills

  • Six Sigma training

  • Familiarity with Minitab Statistical Software

  • CAPA (Corrective Action / Preventive Action) experience

  • Strong written and verbal communication skills

  • Validation Experience (IQ, OQ, TMV, PQ)

For Baccalaureate degrees earned outside of the United States, a degree that satisfies th

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Company

Medtronic

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