Skills this job asks for
Risk managementLean / Six SigmaStatistics
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Sponsorship verdict
Sponsorship possible
One solid signal, not two. Worth applying, and worth asking about sponsorship early.
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✓
Employer is on a government sponsor recordThe US Department of Labor certified 193 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first.
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The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
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No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area.
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✓
What Medtronic INC paid sponsored hires in similar roles3 certified filings for “Principal Systems Engineer” (Electrical Engineers) in MN: $131k–$131k, median $131k.
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Confirmed live todayWhen a source last listed this job as open.
Details and sources
- Employer is on a government sponsor record
- The US Department of Labor certified 193 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. Source: LCA disclosure data (US Department of Labor (OFLC)).
- No salary bar for this route
- H-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- What Medtronic INC paid sponsored hires in similar roles
- 3 certified filings for “Principal Systems Engineer” (Electrical Engineers) in MN: $131k–$131k, median $131k. Most were filed at wage level IV (100%) — 4 lottery entries, ≈61% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.
About the role
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
·And 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.
In general, the following responsibilities apply for the Senior Electrical Engineer role but is not limited to the following:
• 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 I
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