Jobs / United States / Medtronic INC

Medtronic INC

Quality Systems Specialist

Swedesboro, New Jersey, United States of America Posted today

Apply on employer site ↗ Tailor my CV first Source: Company careers site

Optional: we can tailor a CV and cover letter for this job from your real experience first (the first one is free).

Skills this job asks for

ComplianceSupply chainLeadershipProduct managementAudit

Add your CV (free) to see which of these your CV is missing.

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.
  • 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.
  • What Medtronic INC paid sponsored hires in similar roles1 certified filing for “Principal Regulatory Affairs Specialist” (Regulatory Affairs Specialists) in NJ: $102k–$102k, median $102k.
  • 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
1 certified filing for “Principal Regulatory Affairs Specialist” (Regulatory Affairs Specialists) in NJ: $102k–$102k, median $102k. 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 - 5 Nov 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 At Medtronic, you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. The Quality Specialist supports Quality Management System (QMS) execution and quality operations within the Woolwich Distribution Center, ensuring compliance with regulatory requirements, internal quality standards, and Medtronic quality system procedures. This role partners closely with Distribution Operations, Supply Chain, Engineering, Regulatory Affairs, and Quality leadership to support product flow, nonconforming product management, audit readiness, process improvement, and continuous quality initiatives that enable safe and compliant distribution activities. This position is based in Swedesboro, New Jersey and is fully onsite. Approximately 5% travel is required, primarily for training activities. The Quality Specialist serves as a key quality partner to distribution operations, providing day-to-day support for quality systems, compliance activities, product disposition, investigations, audits, and continuous improvement initiatives. This role helps ensure products are managed in accordance with applicable regulatory requirements, internal procedures, and quality standards while supporting efficient distribution center operations.                     Responsibilities may include the following and other duties may be assigned: • Provide daily quality support to distribution operations and serve as a quality resource during operational escalations and issue resolution activities. • Manage Product Hold Orders (PHOs), Return-to-Vendor (RTV) activities, product segregation processes, and disposition of nonconforming products. • Support investigations, containment activities, root cause analysis, and corrective and preventive actions for quality issues. • Maintain and support Quality Management System documentation, including Job Instruction Bulletins (JiBs), work instructions, and controlled documents. • Participate in internal, external, and regulatory audit preparation, evidence collection, response activities, and follow-up actions. • Conduct quality walk-throughs and Gemba activities to identify compliance risks and process improvement opportunities. • Support calibration, environmental monitoring, validation activities, and reporting of quality-related excursions. • Monitor quality metrics and contribute to continuous improvement initiatives focused on compliance, risk reduction, and operational performance. Must Have: Minimum Requirements To be considered for this role, please ensure the minimum requirements are evident in your applicant profile.   • Bachelor's degree and 2+ years of experience in Quality, Manufacturing, Distribution, Supply Chain, or regulated industry environments OR Master's degree and 0 years of experience. Nice to Have • Experience supporting Quality Management System (QMS) processes. • Experience investigating nonconforming products, quality events, or corrective and preventive action activities. • Experience supporting audits, compliance programs, or regulated quality processes. • Exp

Apply on employer site ↗