Quality Technician III

We anticipate the application window for this opening will close on - 21 Aug 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 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 product as part of the complaint handling process. The Technician will be capable of supporting complaint investigations with limited supervision. He or she 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. We believe that when people from different cultures, genders, and points of view come together, innovation is the result — and everyone wins. Medtronic walks the walk, creating an inclusive culture where you can thrive.                     Primary responsibilities apply for the Quality Technician IV role. This includes, but is not limited to the following: • 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: · No minimum education requirement. · Minimum of 3+ 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. 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