Principal Test Method Engineer

Job description

We anticipate the application window for this opening will close on - 19 Oct 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 LifeMedtronic is seeking a Principal Test Method Engineer within the Intervention Cardiology Therapy (ICT) Operating unit focusing on Renal Denervation (RDN). This role will be part of the Design Assurance team and will increase product development process rigor to ensure robust understanding of designs, documentation of compliance to requirements and timely, high-quality product launches that satisfy patient needs and reduce customer complaint rates. This role will have primary focus and responsibility for the validation of design verification test methods for complex electro-mechanical medical devices. This position is based at our Mounds View, MN facility and follows a hybrid work model requiring a minimum of 4 days per week on-site for in-person collaboration. This role may require up to 10% travel to support business objectives, in-person meetings and project activities. Responsibilities may include the following and other duties may be assigned: Lead the team responsible for the validation of Design Verification Test Methods for a new Product Development project for complex electro-mechanical medical device Collaborate cross-functionally with stakeholders (e.g. R&D, clinical, marketing and regulatory) to translate design inputs and real-world clinical use conditions into robust reliable test methods; Drive automation and reduce variability to deliver best-in-class test methods Develop and validate custom test equipment and fixtures, partnering with suppliers where needed Manage capital equipment procurement and financial tracking for equipment and validation activities Lead and contribute to complex test method validation activities - designing studies, executing with precision, and performing data analyses (including gage R&R, ANOVA, and Probability of Misclassification); Lead investigations, refine methods, and ensure compliance with design inputs and international standards Work through extended team members and partner with test labs to facilitate timely completion of test method validation activities in alignment with the overall project phase and project target milestones Communicate progress to project leadership on frequent basis; Distill complex issues into a concise and clear message Required Qualifications: Bachelor's degree in science, technology, engineering, math or related technical field with a minimum of 7 years of technical experience OR Advanced degree in science, technology, engineering, math or related technical field with a minimum of 5 years of technical experience Measurement System Analysis (MSA) and Design of Experiment (DOE) experience Preferred Qualifications: Experience in engineering development with extensive engineering knowledge and skills in some or all of the following: test method development, design for six sigma principles, pre-clinical evaluations, system requirements development, design control, application of ISO standards for medical devices, equipment, process/equipment validation, capital equipment Knowledge in electrical engineering principles Project management experience Medical Device industry experience Familiarity with these regulations: FDA 21 CFR Part 820 cGMP, ISO 13485, ISO 10012, and ISO 17025 Experience in the management of complex data sets and statistical data analysis Ability to manage project timelines to execute deliverables in a timely manner 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 that may be specific to each role. U.S. Work Authorization & Sponsorship At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment. ‌ Recruitment Fraud Alert We are aware of phishing scams targeting job seekers. Please keep the following in mind: Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate. If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments. If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com. ‌ Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Salary ranges for U.S (excl. PR) locations (USD):$132,000.00 - $198,000.00 ‌ This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP). The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others). The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-