Senior Reliability Engineer

Medtronic plc; Mounds View (MN); Hybrid; USD 107,000 - 161,000; Full time

Benefits offered by this job

Health, Dental, Vision Insurance

401(k) with company match

Tuition assistance/reimbursement

Job summary

Medtronic plc is seeking a Senior Reliability Engineer to support post-market quality in the Electrophysiology Therapies Defibrillation Solutions unit. Based in Mounds View, MN, this role requires a hybrid work model with at least four days on-site for collaboration and project execution.

You will analyze product performance data, support risk assessments, and investigate quality issues to improve implantable devices like pacemakers and leads, collaborating with cross-functional teams across

Qualifications

• Bachelor's degree in Engineering, Science, or a technical discipline with 4+ years of related work experience, or 2+ years with an advanced degree.
• Experience in reliability engineering or risk management is preferred.
• Experience with 21 CFR 820, ISO 13485, and ISO 14971 is advantageous.

Responsibilities

• Support reliability and engineering activities to analyze, debug, and recommend design or process changes that improve system reliability.
• Assist with risk analyses to understand how quality issues may affect patient safety.
• Prepare risk assessments, technical reports, and quality documentation; may fulfill the role of Personnel with Clinical Knowledge in risk management.

Skills

Reliability engineering

Root cause analysis

Data analysis

Risk management

Cross-functional collaboration

Education

Bachelor's degree in Engineering/Science

Advanced degree (MS/PhD) preferred

Tools

CRM software

Job description

We anticipate the application window for this opening will close on - 13 Nov 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 LifeThe Senior Reliability Engineer will support key technical activities within the Electrophysiology Therapies (EPT) Defibrillation Solutions (DS) Post Market Quality organization. This role will contribute to post-market surveillance activities by analyzing product performance data, supporting risk assessments and technical documentation, and helping investigate quality issues to improve product performance for implantable products such as pacemakers, defibrillators, and leads.The EPT DS operating unit offers high power devices and therapies to treat abnormal heart rhythms.This position will be 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 and project activities.Primary Responsibilities:Support reliability and engineering activities to analyze, debug, and recommend design or process changes that improve system and process reliabilityAssist with risk analysis studies of designs and processes to understand how potential quality issues may contribute to product quality or patient safety riskAuthor or support the preparation of risk assessments, technical reports, and documentation of analysis results or quality impact; May fulfill the role of “Personnel with Clinical Knowledge” in risk management assessments if specialized skill criteria is metSupport verification and validation of device system requirements, including traceability and testabilityConduct or support evaluation of finished product systems, including requirements, design, development, documentation, integration, test, verification, and validationInterpret and decompose system and product requirements and verify compliance with applicable standards and specificationsCollaborate with cross-functional partners to help investigate quality issues and support corrective actionsAnalyze product performance data and summarize findings to support post-market surveillance and product improvement activitiesPreferred QualificationsUnderstanding of CRM products and their use in the clinical environmentExperience in reliability engineering or risk managementClinical field experience utilizing CRM productsExperience in root cause investigations and assessing the risk impact of proposed design changesExperience with 21 CFR 820, ISO 13485, and ISO 14971Ability to evaluate and debug electrical designs, including RF performanceExperience with design, verification, and validation of Class III medical devices or similar regulated productsDemonstrated ability to perform data analysis using statistical techniques and reliability toolsRequired QualificationsBachelor’s degree in Engineering, Science, or a technical discipline AND 4+ years of related work experience OR 2+ years of related work experience with an advanced degreeFor 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 [e-mail] .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):$107,200.00 - $160,800.00This 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.