Quality Technician III (Medical Device)

We anticipate the application window for this opening will close on - 13 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 a minimum of 4 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. In this exciting role as a Quality Technician III supporting the Cardiac Ablation Solutions organization, you will have responsibility for the inspection and testing of returned products as part of the complaint handling process. The Technician will be capable of supporting complaint investigations with limited supervision. They will exhibit an ability to interact with co-workers in a way that facilitates sharing of information and timely resolution to complaint investigations. The technician shall be capable of using inspection and testing equipment and generating summary reports supporting the analysis results. The Cardiac Ablations Solutions Unit develops life-restoring therapies and healthcare solutions that span the care continuum; integrating technologies and applying clinical and economic evidence to increase patient access, improve efficiency of procedures and deliver successful patient outcomes. This position is in Fridley Creek, in the Rice Creek facility within the Cardiac Ablation Solutions Operating Unit and requires 5 days onsite per week. Primary Responsibilities Experience conducting mechanical and electrical tests Medical device industry experience Execute product Inspection and test plans on bio-hazard product Identify failures, potential causes, and capture the supporting objective evidence Generate product analysis reports Provide support with the development of procedures, processes, tools, and techniques for performing product analysis. Coordinate and link information from multiple sources/systems to analyze problems thoroughly Required Qualifications High School diploma. Minimum of 4 years of relevant work experience and may require vocational or technical education or certification in addition to prior work experience. Preferred Qualifications Medical device industry experience. Familiarity with these regulations: FDA 21 CFR Part 820, EU 217/745 (EU MDR) Familiarity with these standards: ISO 13485, ISO 14971, IEC 60601 Knowledge of Microsoft Office Applications (Word, Excel, Access, and PowerPoint) and Windows OS Strong written and verbal communication skills and ability to work cooperatively as part of a cross-functional team #LI-MDT 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 of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements tha ... (truncated, view full listing at source)