Senior Systems Engineer

Medtronic

Mounds View (MN)

On-site

USD 110,000 - 166,000

Full time

14 days+

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Benefits offered by this job

Health insurance
Dental insurance
Vision insurance
401(k) plan
Paid time off

Job summary

Medtronic's Interventional Cardiac Therapies Renal Denervation group seeks a Sr. Systems Engineer to advance the design and development of next‑gen medical devices.

You will work across software, firmware, hardware, and mechanical domains to accelerate product realization and ensure regulatory compliance. Join a high-performing team dedicated to improving patient outcomes and supporting Medtronic's mission to alleviate pain, restore health, and extend life.

Qualifications

  • Bachelor's degree in Electrical, Computer, Software or Systems Engineering, Physics, or related field.
  • Minimum 4 years integrating and verifying system design functions; advanced degree 2 years; PhD 0 years.
  • Medical device experience and knowledge of design verification is preferred.

Responsibilities

  • Create and execute test suites for integrating and verifying system design functions.
  • Solve complex systems interaction problems in coronary artery disease or renal denervation.
  • Define interfaces between software, firmware, hardware, and mechanical components.
  • Collaborate in cross-functional teams to meet major project objectives.
  • Develop system architecture aligned with business and customer needs.

Skills

Systems engineering
Electrical engineering
Embedded software
Regulatory knowledge
Requirements management

Education

Bachelor's Degree in Electrical, Computer, Software or Systems Engineering, Physics

Tools

MBSE
IEC 60601-1
ISO 13485

Job description

We anticipate the application window for this opening will close on - 31 Aug 2026Careers 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 LifeWe are a learning culture, an inventive and collaborative group. We are dedicated to making sure that every patient gets the best product —when they need it. We have strong ties to our local communities. Our vibrant employee communities respect and value individual experience and perspective as we aim to improve lives and the access to healthcare.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.This position will be based in Mounds View, MNMedtronic’s Interventional Cardiac Therapies (ICT) Renal Denervation (formally CRDN) business is looking for a Sr. Systems Engineer to be part of a high-performing team that is revolutionizing the design and development of medical devices. In this role, you will leverage both your technical breadth and business acumen to accelerate the design and development of next generation of medical devices. The work you do will impact patients globally and help support Medtronic’s mission of alleviating pain, restoring health, and extending life for millions.This engineering position requires strong technical and leadership skills to support the capital equipment development of innovative, new products within the Renal Denervation Group . The Sr. Systems Engineer will apply knowledge of circuit card design, embedded software, and experience in working on complex multidisciplinary problems.Systems Engineering activities typically involve trade-offs between risks, benefits, and performance. Systems Engineering activities are performed within the constraints of a complex regulatory environment, in partnership with development (software, firmware, hardware, mechanical engineering), research, clinical, regulatory, product planning, and marketing groups.The ideal candidate will have a passion for the patients we serve and an unrelenting desire to improve our business. The candidate will be motivated and must have exceptional soft skills that will be used to work with a team.Role and ResponsibilitiesThe candidate will be responsible for creating and executing test suites for integrating and verifying system design functions.Responsibilities may include the following and other duties may be assigned. Use critical thinking skills and technical knowledge to solve complex systems interaction problems in the fields of coronary artery disease or renal denervation.Provide expertise in multiple roles in the product development life cycle through deep knowledge of system functionality including electronics and software.Responsible for completeness and correctness of requirements.Define interface requirements between systems for assigned features (e.g. software, firmware, hardware, mechanical).Participate in cross-functional teams and make appropriate, timely decisions, and recommendations that result in the successful completion of major project objectives.Execute multiple systems engineering activities in the product development life cycle including identification, planning, monitoring, and executing assigned tasks.Collaborate with internal and external stakeholders to develop business and customer needs for new product development.Design or support development of a systems architecture that aligns product development with the needs of the business and the customer.Contribute to defining new technologies through the understanding and utilization of knowledge in product design and in-vivo use conditions.Support or lead key design trade-offs for assigned features, present to project management, and drive decisions. Extensive ability to foresee problems and provide alternate solutions.Apply knowledge of systems engineering principles, competencies, and methodologies.Must Have: Minimum RequirementsTo be considered for this role, please ensure the minimum requirements are evident on your resume.Bachelors degree in Electrical, Computer, Software or Systems Engineering, Physics, or a related degree program requiredMinimum of 4 years of experience integrating and verifying system design functions,Or advanced degree with 2 years of experience integrating and verifying system design functionsOr PhD with 0 years experienceNice to Have (Preferred Qualifications)Medical Device Industry experienceUnderstanding and experience in design, development, and testing of complex medical devices systemsUnderstanding of and experience with developing system requirements, verification protocols, and test methods for embedded medical devicesExperience with IEC 60601-1 and ISO 13485Familiarity with Model Based Systems EngineeringExperience with QMS requirementsExperience with secure by design principlesBasic knowledge of software development and computer programmingWorking knowledge of systems engineering principles, requirements management, task management, and medical device regulationDemonstrated ability to build strong relationships at all levels of the organization, cross-functionally, and with key people external to the organizationFor 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 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.U.S. Work Authorization & SponsorshipAt 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 AlertWe 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 & CompensationMedtronic offers a competitive Salary and flexible Benefits PackageA 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):$110,400.00 - $165,600.00This 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-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:Medtronic benefits and compensation plansIt 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.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 here 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.
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