Supplier Quality Engineer II - Brooklyn Park, MN

We anticipate the application window for this opening will close on - 18 Nov 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 The Supplier Quality function supports enterprise operations by partnering with suppliers and cross-functional engineering and manufacturing teams to ensure purchased parts, materials, and services meet quality requirements throughout the product lifecycle. This Supplier Quality Engineer II position is based at Medtronic’s Brooklyn Park, Minnesota site and supports enterprise operations through supplier qualification, New Product Development, manufacturing support, and continuous improvement activities in a regulated medical device environment. This position requires onsite work five days per week. As a Supplier Quality Engineer II, you will support supplier quality activities from supplier qualification through manufacturing, with potential involvement in New Product Development (NPD). You will monitor supplier performance, address quality issues, conduct supplier audits, and partner with Component Engineering and other quality teams to ensure purchased components meet applicable quality and regulatory requirements. Primary Responsibilities Ensure suppliers deliver parts, materials, and services that meet established quality requirements. Qualify suppliers according to company standards and support receiving inspection and supplier quality programs. Monitor supplier parts throughout the manufacturing cycle and drive resolution of supplier-related quality issues. Develop and prioritize supplier audit schedules and conduct audits against Good Manufacturing Practice (GMP) and applicable quality standards. Evaluate supplier processes and quality systems, communicate findings, and drive appropriate improvements. Provide Supplier Quality Engineering support throughout the New Product Development lifecycle for newly qualified parts. Partner with Component Engineering and Post-Market Supplier Quality teams on product acceptance sampling strategies, Approved Supplier List coordination, Supplier Owned Quality deployment, and control plans. Define receiving inspection requirements and support validation of applicable internal test methods. Required Qualifications Bachelor’s degree in Engineering, Science or technical field and 2+ years of relevant experience OR master's degree in Engineering, Science or technical field with 0+ years of relevant experience. Preferred Qualifications Medical device industry experience and working knowledge of ISO 13485, ISO 14971, and 21 CFR Part 820. Experience applying Define, Measure, Analyze, Improve, and Control (DMAIC) or Lean Six Sigma principles; Green Belt or Black Belt certification preferred. Statistical data analysis experience, including Statistical Process Control (SPC), root cause analysis, and problem-solving methodologies. Experience with risk management, Corrective and Preventive Action (CAPA), or Automated Optical Inspection (AOI) validation. Experience interfacing with internal customers, suppliers, and external regulatory agencies. For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 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…

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