We anticipate the application window for this opening will close on - 30 Aug 2025  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.<h1>A Day in the Life</h1><div><div>In this exciting role as a Principal Electrical Engineer within Medtronics Coronary &amp; Renal Denervation Operating Unit, youll be an integral part of the Design Assurance team. Our purpose is to 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. You will have primary focus and responsibility for the validation of design verification test methods for complex electro-mechanical medical devices. </div><div>Medtronic’s Coronary and Renal Denervation (CRDN) business is looking for a Principal Electrical Engineer to be part of a high-performing team that is revolutionizing the design and development of energy based therapeutic medical devices to treat hypertension. In this role, you will leverage both your technical breadth and business acumen and participate in the design and development of next generation medical devices. </div><div> </div><div>Join a diverse team of innovators who bring their worldview, their unique backgrounds, and their individual life experiences to work every day. It’s no accident — we work hard to cultivate a workforce that reflects our patients and partners. We believe it’s the only way to drive healthcare forward and remain a global leader in medical technology and solutions. To learn more about Inclusion &amp; Diversity at Medtronic <a href="https://www.medtronic.com/us-en/about/careers/diversity-inclusion.html" target="_blank">Click Here</a> 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. </div><div>Location: Mounds View, MN. </div><div>Travel up to 10%. </div><div>A Day in the Life </div><div>Responsibilities may include the following and other duties may be assigned. </div><div><ul><li>Responsible for leading the team that is responsible for the validation of Design Verification Test Methods for a new Product Development project for complex electro-mechanical medical devices. Candidate should have experience developing/validating electrical system and subsystem test methods, preferably with an electronic engineering background. </li></ul></div><div><ul><li>Work within the Design Assurance team and cross-functionally with R&amp;D, clinical, marketing and regulatory to translate design inputs and clinical use conditions into test methods - meeting all stakeholders’ requirements. </li></ul></div><div><ul><li>Support the development and own the validation of test equipment and fixtures, and where required work closely with suppliers to validate equipment to Medtronic requirements. Manage capital equipment procurement and financial tracking for Design Verification equipment. Automate testing and reduce test method variation to ensure robust and appropriate test methods to demonstrate compliance to Design Inputs. </li></ul></div><div><ul><li>Lead and successfully complete complex test method validation tasks including operator training, determining appropriate validation study design and sample size, data analysis including crossed gage R&amp;R, ANOVA, Probability of Misclassification, identification and reduction of sources of variation and report writing for system and capital equipment test methods. </li></ul></div><div><ul><li>Liaise with extended team members, test lab managers and test operators, to facilitate timely completion of test method validation activities in alignment with the overall project phase and project target milestones. </li></ul></div><div><ul><li>Provide technical expertise in test method development, exhibit strong problem-solving skills, support project investigations and lead validation activities in alignment with the overall project phase and project target milestones. </li></ul></div><div><ul><li>Communicate progress to project leadership on frequent basis. Be able to distill complex issues into concise and clear messages. </li></ul></div><div><ul><li>As part of ongoing professional development, you will maintain expert, up to date knowledge of developments in regulatory compliance requirements for product design, development, transfer, and commercialization activities. </li></ul></div><div><ul><li>Translate international standards requirements and regulatory guidance into test methods. </li></ul></div><div><ul><li>Work independently to plan and schedule the test method team’s and your own activities necessary to meet timelines. </li></ul></div></div><div><div>  </div><div>Must Have (Minimum Requirements): </div><div>To be considered for this role, the minimum requirements must be evident on your resume.  </div><div><ul><li>Bachelors degree in science, technology, engineering, math or related technical field with a minimum of 7 years of technical experience OR Advanced degree with a minimum of 5 years of technical experience </li></ul></div><div>Nice to Have (Preferred Qualifications): </div><div><ul><li>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, capital equipment. </li></ul></div><div><ul><li>Experience in electrical engineering principles is essential </li></ul></div><div><ul><li>Practical knowledge of project management. </li></ul></div><div><ul><li>Medical Device Industry experience. </li></ul></div><div><ul><li>Familiarity with these regulations: FDA 21 CFR Part 820 cGMP, ISO 13485, ISO 10012, and ISO 17025. </li></ul></div><div><ul><li>Experience in the management of complex data sets and statistical data analysis. </li></ul></div><div><ul><li>Ability to manage project timelines to execute deliverables in a timely manner. </li></ul></div></div>Physical Job RequirementsThe 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.<h1>Benefits &amp; Compensation  </h1>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):$124,800.00 - $187,200.00This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).<h2></h2><h2></h2>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-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums). Regular employees are those who are not temporary, such as interns.  Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico. Further details are available at the link below:<a href="https://www3.benefitsolver.com/benefits/BenefitSolverView?page_name=signon&amp;co_num=30601&amp;co_affid=medtronic" target="_blank">Medtronic benefits and compensation plans</a><h1>About Medtronic</h1><h1></h1>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.  We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.Learn more about our business, mission, and our commitment to diversity <a href="http://www.medtronic.com" target="_blank">here</a>.It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.<div><div><div><div><div><div><div>If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find <a href="https://www.medtronic.com/content/dam/medtronic-wide/public/united-states/employee-support-services/careers/la-county-legal-notice.pdf" target="_blank">here</a> a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.</div></div></div></div></div></div></div>