Jobs / United States / Medtronic INC
Senior Supplier Quality Engineer - Grand Rapids, MI
Medtronic INC · 🇺🇸 Grand Rapids, Michigan, 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 roles16 certified filings for “Sr. Supplier Quality Engineer” (Industrial Engineers) in MN: $109k–$124k, median $109k. Most were filed at wage level III (44%) — 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 - 11 Sep 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 Grand Rapids, Michigan manufacturing site produces approximately 600 finished products, including cannulae and beating heart products used across Medtronic’s cardiovascular portfolio. The Supplier Quality Engineering function partners closely with suppliers and cross-functional teams to ensure purchased materials, components, and finished devices meet quality, regulatory, and operational requirements throughout the product lifecycle. This position is based in Grand Rapids, MI and requires onsite work five (5) days per week to support supplier quality activities, manufacturing operations, and cross-functional collaboration. This role has minimal travel. As a Senior Supplier Quality Engineer, you will support supplier quality management activities for purchased materials and components used in manufacturing. This role is responsible for supplier performance oversight, investigation of supplier-related quality issues, implementation of supplier controls, and support of product and process changes to ensure compliance with quality system and regulatory requirements. Primary Responsibilities: • Manage supplier quality performance and monitor supplier compliance with quality requirements for materials, components, and services. • Lead investigations related to supplier quality issues, nonconforming materials, Supplier Corrective and Preventive Actions (CAPAs), Material Review Board activities, and inspection findings. • Coordinate supplier onboarding activities, including Approved Supplier List (ASL) additions and supplier setup across applicable quality and business systems. • Partner with engineering and cross-functional teams to develop product acceptance strategies, supplier control plans, and quality requirements for new products and processes. • Define receiving inspection requirements and support validation of internal test methods associated with supplied products. • Evaluate supplier change notifications and assess potential impacts to manufacturing operations, inventory, acceptance activities, and product configurations. • Apply statistical quality techniques to analyze supplier performance, identify trends, and implement corrective actions. • Drive continuous improvement initiatives using Lean, Six Sigma, Kaizen, and other quality improvement methodologies. Required Qualifications: • Requires a Bachelor’s Degree in Engineering, Science or technical field with 4+ years of work experience in Engineering and/or Quality OR Advanced Degree in Engineering, Science or technical field with 2+ years of work experience in Engineering and/or Quality OR PhD with 0 years relevant experience. Preferred Qualifications: • Experience investigating quality issues, nonconforming products, corrective actions, or supplier-related quality concerns. • Knowledge of quality systems, regulated manufacturing environments, or supplier quality processes. • Ability to analyze data and apply problem-solving methodologies to support quality and process improvements. • Experience in supplier quality engineering within the medical device industry or another regulated manufacturing environment. • Working knowledge of Quality System Regulation (21 CFR Part 820