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Medtronic10K+ employees

Assoc Quality Systems Specialist - Japanese Language

Location not statedSalary not listedPosted yesterday

Immigration summary

Visa sponsorship

LikelyHigh confidence

This employer has recently sponsored work like this.

287 recent H-1B filings · 1 similar-role filing

View visa evidence

Green card sponsorship

Strong historyMedium confidence

This employer has recently sponsored green cards at scale.

77 recent certified PERM filings

View green card evidence

Job description

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 Associate Quality Systems Specialist will be part of the Regional Quality team responsible for end-to-end compliant handling. This role will be located in BGC, Taguig City, Philippines.

The process may include ones that requires translation English to Japanese, or Japanese to English. The role is expected to communicate with internal stakeholders located both in Japan and outside the country but within the organization. Majority of communication is being made by writing (such like email, Microsoft Teams), with regular team meetings held in Japanese.

Primary Responsibilities

  • Entering incoming potential compliant information into designated complaint handling system
  • Executing attempts for follow-up information
  • Delivery customer letters
  • Other processes in complaint handling

Required Qualifications

  • Bachelor’s Degree in any field is required
  • 0-2 years of relevant experience or related role within the Medical Device industry (Regulatory and Quality role)
  • Able to communicate in both English and Japanese (N4 or above certification) as the role will require communication with stakeholders from Japan

Preferred Qualifications

  • Good understanding of ISO Quality Management Systems (ISO 9001, 13485)
  • Experience working in Medical device industry
  • Related experience in Quality or Regulatory roles

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

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Recruitment Fraud Alert

We are aware of phishing scams targeting job seekers. Please keep the following in mind:

Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.

Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate.

If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments.

If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com.

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package

A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.  We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).

Sponsorship evidence

Why Openbound reached the conclusions above.

Visa sponsorship evidence

Current posting

Silent on sponsorship

Other openings

10 of 619 recent openings at this employer state a sponsorship restriction.

Employer H-1B history

287
recent certified H-1B filings
110
new-hire petitions
1
filings for similar roles
211
so far in FY2026

Filed titles like this role: quality systems specialist

More evidence details
  • 1 certified H-1B filing for this same role
  • 287 recent certified H-1B filings across the employer
  • Still filing this year — 211 filings in FY2026
  • 100 USCIS H-1B new-employment approvals, counted separately from LCA filings
  • 614 further USCIS approvals for extensions or transfers
  • 10 other recent postings at this company state a sponsorship restriction
  • The posting says nothing about sponsorship either way
  • No filing activity is recorded for this job's location

Green card sponsorship evidence

Employer PERM history

77
recent certified PERM filings
0
filings for similar roles
Certified PERM filings by fiscal year
202357
202489
202577
202677YTD

Filing history reflects past employer behavior; it isn't a promise for this opening.

All open roles at Medtronic
How Openbound evaluates sponsorship

Visa history uses official U.S. Department of Labor H-1B LCA disclosure data and USCIS H-1B petition history. Green card history uses DOL PERM disclosure data. Each is read for the employer as a whole, for roles like this one, and for this location, weighted toward the most recent fiscal years.

An employer is matched to its filing entities by verified legal name and reviewed aliases; a match is never made on a name resemblance alone. Where no verified entity can be matched, the page says so and draws no conclusion from the absence. 335 filing titles were examined for this employer.

What this posting states outranks history in both directions, and an employer's published policy outranks past filings. Filing history reflects past behavior; it is not a promise of sponsorship for this opening, and none of this is legal advice.