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Senior Electrical Engineer

Job in Mounds View, Ramsey County, Minnesota, USA
Listing for: Medtronic plc
Full Time position
Listed on 2026-10-22
Job specializations:
  • Engineering
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 108000 - 162000 USD Yearly USD 108000.00 162000.00 YEAR
Job Description & How to Apply Below

We anticipate the application window for this opening will close on - 30 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 Life

Medtronic is seeking a Senior Electrical Engineer to support the Electrophysiology Therapies (EPT) Operating Unit. This role will have responsibility for ensuring our products exceed the safety and reliability requirements and expectations of patients, clinicians, regulators, and the business. The EPT Operating Unit offers devices and therapies that treat patients with abnormal heart rhythms and heart failure. It is comprised of 4 businesses:

  • Cardiac Pacing Therapies
  • Cardiovascular Diagnostic & Services
  • Defibrillation Solutions
  • Cardiac Ablation Solutions

This position is based at our Mounds View, MN facility and requires a minimum of 4 days per week on-site to support collaboration, innovation, and cross-functional partnership. The role also requires 10% or less travel to support project execution, business needs, and collaboration with internal and external stakeholders.

Responsibilities
  • Collaborate with cross-functional teams to develop and release new cardiac rhythm management products and design changes
  • Plan, lead, and integrate Design for Reliability (DfR) activities on product development projects to drive product safety, complaint reduction, reliability, and quality outcomes that exceed patient, customer, company, and regulatory agency expectations
  • Evaluate designs for potential failure modes, assess potential hazards and harms, prioritize safety risks, identify appropriate risk controls, and compile evidence to demonstrate benefits outweigh product risks
  • Define and allocate reliability requirements and goals, develop and lead reliability demonstration strategies, manage completion of reliability growth activities, and recommend design and manufacturing updates to ensure design achieves required levels of product reliability
  • Understand legacy product performance and incorporate learnings into new product development projects
  • Develop test plans, determine statistically valid sample sizes, work with test labs to demonstrate performance, address test observations, statistically analyze data, and write test reports
  • Articulate risk management and reliability activities and conclusions in documentation, regulatory submissions, and audits
  • Perform engineering reviews of quality records for safety and reliability impact
  • Advocate for safety, reliability, and quality in design reviews and other project meetings
Required Qualifications
  • Bachelor’s degree in Science, Technology, Engineering, Math or related technical discipline AND a minimum of 4 years of experience OR a Master's degree with a minimum of 2 years technical experience
Preferred Qualifications
  • Experience applying Six Sigma development methods, such as Design of Experiments (DOE), Robust Characterization (P-Diagram), and Capability Analysis is a plus
  • Strong circuit analysis and hands-on electrical testing experience
  • Experience using design verification and troubleshooting skills, coupled with a working knowledge of quality and statistical methods.
  • Experience writing engineering documents (test plans, reports etc)
  • Medical Device Industry experience or other regulated industry
  • Familiarity with these regulations: FDA 21 CFR Part 820 cGMP, ISO 13485, ISO 14971 and ISO 5841-2 ASQ
  • CRE Certified
  • For…
Position Requirements
10+ Years work experience
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