Quality Engineer II

We anticipate the application window for this opening will close on - 19 Apr 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 4 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. In this exciting role as Quality Engineer II, you will be a part of the Americas Service & Repair team at our Louisville, CO site. Service of medical devices is crucial to ensuring their safe and effective operation, which ultimately allows healthcare professionals to deliver reliable and high-quality care to their patients. You will be an integral part of the team that supports the company’s quality policy to Put Patients First. This team collaborates with global teams to support products across several portfolios in Medtronic. Re sponsibilities may include the following and other duties may be assigned: Develops, modifies , applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product. 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. Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications. Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements. May specialize in the areas of production control, product evaluation and reliability, and/or inventory control as they apply to product or process quality. Implement corrective and preventive actions (CAPA) to address quality issues and ensure documentation is complete and compliant with requirements . Support production control, product evaluation, reliability analysis, and continuous improvement initiatives across assigned product or process areas . Support virtually the Quality Walks Improve Quality (QWIQ ) program at Louisville depot. Support NCMRS (nonconformances) for the Louisville depot. Conduct Material Review Board (MBR) meetings for Louisville depot. Required Knowledge and Experience: Bachelor’s degree in engineering or a Science-related field, with 2 years of relevant experience in Engineering and/or Quality; OR Master's degree with a minimum of 0 years relevant experience. Nice to Have: Training or experience in Root Cause Analysis , NCMRs, and Audit Readiness (internal and external audits) . ​ Nonconformances and CAPA (Corrective Action and Preventive Action) experience. Demonstrated experience with CAPA management and quality system improvements . Experience creating, implementing, and maintaining process improvements, documentation, and change controls . Experience in manufacturing envir onment within Medical Devices or Pharmaceutical industries. 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 descri ... (truncated, view full listing at source)