Jobs / United States / Medtronic INC
Principal Medical Safety Specialist
Medtronic INC · 🇺🇸 Minneapolis, Minnesota, United States of America
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- 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. USCIS also records 106 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- 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. 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 roles3 certified filings for “Senior Risk Management Specialist” (Mechanical Engineers) in MN: $109k–$126k, median $109k. Most were filed at wage level III (67%) — 3 lottery entries, ≈46% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- Confirmed live todayWhen a source last listed this job as open.
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.
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Sponsor Radar — Medtronic INC
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. USCIS also records 106 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Medtronic INC →
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 The Medical Safety team provides clinical expertise and patient safety oversight across the product lifecycle, partnering with Research & Development, Quality, Regulatory Affairs, Clinical, Risk Management, and Post-Market Vigilance teams. The Cardiac Rhythm Management Medical Safety team evaluates product performance, safety signals, adverse events, and emerging risks to support evidence-based decision-making and help ensure the safety and effectiveness of cardiac rhythm technologies. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. This position is remote to enhance our competitive edge and expand our cross-functional collaboration efforts. This role will require up to 10% of travel to enhance collaboration and ensure successful completion of projects. As a Principal Medical Safety Specialist, Cardiac Rhythm Management, you will provide clinical and technical expertise to support patient safety activities across Cardiac Implantable Electronic Device (CIED) therapies and products. You will evaluate safety information, assess potential risks, support post-market surveillance activities, and collaborate with cross-functional partners to inform safety-related decisions throughout the product lifecycle. Primary Responsibilities • Evaluate safety events, adverse event trends, and potential safety signals identified through Quality, Clinical, and Regulatory processes. • Conduct medical safety assessments using complaint data, scientific literature, registries, and post-market surveillance information. • Apply Cardiac Implantable Electronic Device (CIED) expertise to support patient safety evaluations and product lifecycle decision-making. • Respond to safety-related inquiries from internal stakeholders, healthcare professionals, and regulatory agencies. • Collaborate with Medical Safety, Clinical, Regulatory Affairs, Risk Management, and Quality teams to assess and address emerging safety concerns. • Maintain expertise in assigned therapies, products, scientific literature, regulatory requirements, and industry standards. • Provide evidence-based medical input to support safety reviews, risk assessments, and regulatory reporting activities. • Lead or support initiatives that improve safety practices, business processes, and cross-functional decision-making. Required Qualifications • Bachelor's degree in Nursing or healthcare-related field and active healthcare professional licensure. • Minimum of 7 years of Cardiac Implantable Electronic Device (CIED) management experience OR advanced degree and 5+ years of related experience. • Experience in Medical Safety, Medical Affairs, Clinical Management, or related clinical healthcare functions. • Knowledge of CIED therapy management, device programming, remote monitoring, cardiac rhythm interpretation, and associated cardiac disease states. • Experience evaluating clinical, safety, or post-market data to support risk-based decision-making. Preferred Qualifications • Experience with Medtronic programmer platforms, including SmartSync, CareLink 2090, or CareLink Encore. • International Board of Heart Rhythm Examiners (IBHRE) certi