Regulatory Jobs
Hero Gradient Background
Medtronic's glass and brick headquarters building in Galway, Ireland, under a blue sky
Medtronic logo

New · posted Oct 14

Medtronic · Medical Devices

Supplier Quality Engineer II

  • Remote, US
  • Remote
  • Full-time
  • Senior & Principal
Save
EmploymentFull-time
LocationRemote, USRemote
Deadline

Closes Oct 21, 2026 · 8 days left

The role

We anticipate the application window for this opening will close on - 21 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.

What you need

Required Qualifications

  • Bachelor’s Degree in Engineering, Science or technical field with 2+ years of work experience in Engineering and/or Quality OR Advanced Degree in Engineering, Science or technical field with 0+ years of work experience in Engineering and/or Quality
  • Experience working within the medical device, pharmaceutical, biotechnology, or other highly regulated industry.

Preferred Qualificationsnice to have

  • Experience working with supplier quality systems, quality audits, corrective and preventive actions (CAPA), and change management processes.
  • Experience supporting Contract Manufacturers (CMs), Original Equipment Manufacturers (OEMs), or external supplier networks.
  • Experience supporting regulated products within a quality-controlled manufacturing environment.
  • Knowledge of root cause analysis methodologies and continuous improvement tools.
  • Knowledge of FDA Quality System Regulation (21 CFR Part 820), ISO 13485, and risk management principles.
  • Experience conducting supplier audits and leading supplier quality improvement initiatives.
  • Certification as a Quality Engineer, Auditor, or related quality professional certification.

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.

What you'll do

This role supports Supplier Quality within Medtronic, partnering with Contract Manufacturers (CMs), Original Equipment Manufacturers (OEMs), and sub-tier suppliers to ensure the quality, compliance, and continuous improvement of supplied medical devices and components. The team collaborates closely with Research & Development, Quality, Regulatory, and supplier partners to maintain effective quality systems, support product and process changes, and drive supplier performance across the product lifecycle.

This is a U.S. Remote position. Candidates may be located anywhere within the United States but preference is the Midwest. Travel of up to 15% is required to support supplier visits, audits, business reviews, and cross-functional activities.

The Supplier Quality Engineer II is responsible for managing supplier quality activities for Contract Manufacturers and Original Equipment Manufacturers, ensuring supplied products and processes meet Medtronic quality, regulatory, and customer requirements. This role partners with internal and external stakeholders to support product and process changes, monitor supplier performance, implement corrective actions, and drive continuous improvement across the supply base.

  1. Manage supplier quality relationships with Contract Manufacturers (CMs), Original Equipment Manufacturers (OEMs), and sub-tier suppliers to ensure compliance with quality and regulatory requirements.
  2. Support supplier-related product and process changes through effective quality planning, risk assessment, validation, and change control activities.
  3. Monitor supplier quality performance using established metrics and lead improvement initiatives to address quality, delivery, and compliance concerns.
  4. Conduct supplier audits, assessments, and business reviews to evaluate quality system effectiveness and identify opportunities for improvement.
  5. Investigate quality issues, facilitate root cause analysis, and drive corrective and preventive actions with suppliers and internal stakeholders.
  6. Partner with Research & Development, Quality, Regulatory, Operations, and Manufacturing teams to ensure supplied products meet finished device requirements.
  7. Review and approve supplier quality documentation, including nonconformance investigations, corrective actions, process validations, and change notifications.
  8. Ensure supplier activities comply with applicable medical device regulations, industry standards, and internal quality system requirements.

Pay and benefits

$80,000 – $120,000 a year

Employer provided
How this compares

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.

Salary ranges for U.S (excl. PR) locations (USD):$80,000.00 - $120,000.00

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).

The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).

Regular employees are those who are not temporary, such as interns.  Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.

Further details are available at the link below:

Medtronic benefits and compensation plans

If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. Medtronic will consider for employment qualified job applicants with arrest or conviction records in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

  • Health, dental and vision insurance

  • 401(k) with employer contribution and match

  • Paid time off

  • Employee Stock Purchase Plan

  • Tuition assistance

  • Incentive plan (MIP)

Working conditions

U.S. Work Authorization & Sponsorship

At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.

Equal opportunity, accessibility and legal noticesMedtronic's statements, word for word

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 [email protected].

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.

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

Job intelligence

The context around this role

Live data · October 14, 2026

Salary intelligence

How the pay compares

This role's midpoint is 20% below the US median for Quality Assurance roles at this level.

This roleEmployer provided

$80,000 to $120,000 a year

Senior & Principal roles in the US221 roles publishing pay

Middle half $105,500 to $142,000, median $124,500
Annual base pay
Annual base payLowMedianHigh
This role$80,000—$120,000
All US$105,500$124,500$142,000

This role: Medtronic's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 14, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Assurance

The general path across 598 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Medtronic's own promotion track.

  1. One step back

    Associate & Specialist

    Often: Quality Engineer · Intern

    $80K median156 open
  2. This role

    Senior & Principal

    Often: Quality Engineer · Supplier Quality Engineer

    $125K median269 open
  3. Next step

    Manager

    Often: Manager, Quality Assurance · QA Supervisor

    $156K median92 open
  4. Later

    Director

    Often: Associate Director · Associate Director, GMP Operational Quality

    $211K median69 open
  5. Later

    VP & Executive

    Often: AVP · Executive Director Quality, Cell & Gene Therapy

    $293K median12 open

Skills DNA

What this role leans on

How many of the posting's 23 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 10 linesLab testing and methods: 1 lineDocumentation and SOPs: 1 lineInvestigations and CAPA: 4 linesValidation and qualification: 2 linesQuality systems and risk: 15 linesCollaboration and leadership: 7 linesGMPLab testingDocumentationInvestigationsValidationQuality systemsTeamwork
  • Quality systems and risk15
  • GMP and compliance10
  • Collaboration and leadership7
  • Investigations and CAPA4
  • Validation and qualification2
  • Lab testing and methods1
  • Documentation and SOPs1

Company hiring pulse

Medtronic on Regulatory Jobs

23
Open roles
18
Distinct roles
11
Locations

By discipline

  • Quality17 74%
  • Regulatory6 26%

By level

  • Senior & Principal18 78%
  • Associate & Specialist4 17%
  • Manager1 4%
See all 23 Medtronic roles

More roles at Medtronic

All 23 Medtronic roles

Similar Quality Assurance roles elsewhere

Supplier Quality Engineer II at Medtronic

Applications close October 21. $80K–$120K a year, employer provided.

Job alerts
    Supplier Quality Engineer II at Medtronic — Remote, US | Regulatory Jobs