Jobs / United States / Medtronic INC
Senior Medical Safety Specialist
Medtronic INC · 🇺🇸 Mounds View, 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 - 4 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 Coronary and Renal Denervation Medical Safety team supports patient safety activities across the product lifecycle, partnering with Clinical, Regulatory Affairs, Quality, Risk Management, Medical Affairs, Product Development, and Post-Market Vigilance teams. The team evaluates safety data, assesses potential safety signals, supports risk management activities, and provides medical expertise to guide safety-related decision-making for coronary artery disease and renal denervation therapies. 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 10% of travel to enhance collaboration and ensure successful completion of projects. As a Senior Medical Safety Specialist, you will provide clinical and medical expertise to support patient safety activities across coronary and renal denervation therapies. You will evaluate safety information, assess potential safety signals, contribute to risk management activities, and collaborate with cross-functional teams to support product safety throughout the product lifecycle. Primary Responsibilities • Evaluate adverse events, complaint data, literature, registries, and other safety information to identify and assess potential safety signals. • Author medical safety assessments and recommendations to support product safety reviews and regulatory reporting activities. • Provide medical and clinical input to Quality, Regulatory Affairs, Risk Management, Clinical, Medical Affairs, and Product Development teams. • Assess and escalate emerging safety concerns and support investigations, risk assessments, and corrective actions. • Perform qualitative and quantitative analyses of post-market safety data and contribute to annual and periodic regulatory reports. • Support responses to safety-related inquiries from internal stakeholders, healthcare professionals, regulatory agencies, and health organizations. • Maintain expertise in assigned therapies, product technologies, applicable regulations, and risk management processes. • Lead initiatives that enhance safety practices, improve business processes, and support evidence-based decision-making across the organization. Required Qualifications • Bachelor's degree in Nursing or a healthcare-related field and licensed healthcare professional status. • Minimum of 4 years of experience in coronary artery disease and renal denervation management OR advanced degree with 2+ years of related experience. • Knowledge of coronary artery disease, hypertension management, and interventional cardiology technologies including balloons, catheters, stents, or renal denervation devices. • Experience in Medical Safety, Medical Affairs, Clinical Research, Clinical Management, or related healthcare functions. • Experience evaluating clinical or post-market safety data and supporting patient safety activities. Preferred Qualifications • Medical device industry experience supporting cardiovascular, coronary, or renal denervation therapies. • Experience with risk management, post-market vig