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Reliability Engineer II
Medtronic. Support reliability and engineering activities to analyze, debug, and recommend design or process changes that improve system and process reliability .
Posted 10/6/2026full-timeMounds View • Minnesota • United StatesJuniorMid-Level💰 $84,800 - $127,200 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in reliability engineering, risk management, and compliance with medical device regulations. Proficient in analyzing product performance data and conducting risk assessments to enhance patient safety and product quality.
Highest-signal resume keywords
Reliability EngineeringRisk ManagementClinical Field ExperienceData Analysis Using Statistical TechniquesDesign Verification and Validation
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Electrical Design EvaluationRoot Cause InvestigationStatistical AnalysisVerification and Validation of Class III Medical DevicesRisk Assessment
Tools & Technologies
Reliability ToolsStatistical Techniques
Industry Keywords
21 CFR 820ISO 13485ISO 14971CRM ProductsPost Market Surveillance
About the role
Key responsibilities & impact- Support reliability and engineering activities to analyze, debug, and recommend design or process changes that improve system and process reliability
- Assist with risk analysis studies of designs and processes to understand potential quality and patient safety risks
- Author or support risk assessments, technical reports, and documentation of analysis results or quality impact
- Potentially fulfill the role of “Personnel with Clinical Knowledge” in risk management assessments if specialized skill criteria are met
- Support verification and validation of device system requirements, including traceability and testability
- Conduct or support evaluation of finished product systems across requirements, design, development, documentation, integration, testing, verification, and validation
- Interpret and decompose system and product requirements and verify compliance with applicable standards and specifications
- Collaborate with cross-functional partners to investigate quality issues and support corrective actions
- Analyze product performance data and summarize findings for post-market surveillance and product improvement activities
- Support technical activities within the EPT Defibrillation Solutions Post Market Quality organization for implantable products such as pacemakers, defibrillators, and leads
Requirements
What you’ll need- Bachelor’s degree in Engineering, Science, or a technical discipline
- Minimum of 2 years of work experience in Engineering, Science, or a related technical field OR minimum of 0 years of work experience with an advanced degree in Electrical Engineering, Engineering, Science, or a related technical discipline
- 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
- Understanding of CRM products and their use in the clinical environment
- Experience in reliability engineering or risk management
- Clinical field experience utilizing CRM products
- Experience in root cause investigations and assessing the risk impact of proposed design changes
- Experience with 21 CFR 820, ISO 13485, and ISO 14971
- Ability to evaluate and debug electrical designs, including RF performance
- Experience with design, verification, and validation of Class III medical devices or similar regulated products
- Demonstrated ability to perform data analysis using statistical techniques and reliability tools
- Unrestricted U.S. work authorization at the time of hire and for the duration of employment
Benefits
Comp & perks- 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
- Simple Steps (global well-being program)
- 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)
- Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums)
- Temporary employees are eligible for paid sick time, as required under applicable state law
- Equal employment opportunity and reasonable accommodations for qualified individuals with disabilities