Senior Supplier Quality Engineer

Medtronic plc; Mounds View (MN); On-site; USD 99,000 - 149,000; Full time

Benefits offered by this job

Health, Dental and Vision insurance

Health Savings Account

Tuition assistance/reimbursement

Employee Stock Purchase Plan

401(k) plan plus employer match

Job summary

Medtronic plc seeks a Senior Supplier Quality Engineer to drive supplier transfers and lifecycle changes across multiple sites in the U.S. You will define qualification plans, execute product qualification, and ensure compliance with FDA/ISO standards.

This onsite role emphasizes collaboration with suppliers and internal teams to mitigate risks and improve quality. Responsibilities include PPAP planning, acceptance strategies, and coordinating ASL activities while guiding product validations and

Qualifications

• Bachelor’s degree in Engineering, Science, or a technical field with 4+ years in a regulated industry.
• Advanced degree with 2+ years in a regulated industry or PhD.
• Experience with supplier controls and PPAP processes is preferred.

Responsibilities

• Define component qualification strategies and PPAP requirements.
• Execute supplier product qualification activities for conforming deliveries.
• Provide quality engineering guidance and compliance oversight across lifecycle.
• Develop acceptance sampling strategies and ASL coordination for transfers.
• Review engineering changes, test methods, and lifecycle deliverables.
• Collaborate with suppliers and cross-functional teams on transfers and improvements.

Skills

Quality engineering

Supplier collaboration

Risk assessment

Education

Bachelor's degree in Engineering/Science

Advanced degree / PhD

Tools

Windchill

Agile PLM

Minitab

Job description

We anticipate the application window for this opening will close on - 16 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

The Senior Supplier Quality Engineer will support the Global Supplier Quality Supplier Change Implementation function, with a focus on supplier transfers, component qualification, supplier quality controls, and product acceptance activities for medical devices.

This role is based in either Mounds View, MN, North Haven, CT or Memphis, TN and requires working onsite a minimum of four days per week. Periodic travel to supplier and Medtronic facilities is expected, less than 25%.

The Senior Supplier Quality Engineer will lead quality activities supporting supplier transfers and product lifecycle changes. This role partners with suppliers and cross-functional teams to define qualification and acceptance strategies, execute supplier and product validations, assess supplier performance, and ensure compliance with applicable quality requirements throughout design transfer and manufacturing.

Primary Responsibilities

• Define component qualification strategies, including Production Part Approval Process (PPAP) requirements, qualification plans, control plans, and release readiness.
• Execute supplier product qualification activities to ensure suppliers can consistently deliver conforming products and materials.
• Provide quality engineering guidance and compliance oversight for supplier activities throughout the product lifecycle.
• Develop and execute product acceptance strategies, sampling plans, and associated test method validation activities at suppliers.
• Evaluate supplier processes and quality systems, assess performance, and provide feedback to address identified risks or performance gaps.
• Develop Product Acceptance Sampling strategies and coordinate Approved Supplier List (ASL) activities for transferred products.
• Review and approve applicable engineering changes, test methods, test equipment, and component engineering lifecycle deliverables.
• Partner with suppliers and cross-functional teams on supplier transfers, process improvements, corrective actions, and quality performance.

Required Qualifications

• Bachelor’s degree in Engineering, Science, or a technical field with 4+ years of experience in a regulated industry OR advanced degree in Engineering, Science, or a technical field with 2+ years of experience in a regulated industry OR PhD.

Preferred Qualifications

• Experience with supplier controls, Approved Supplier List (ASL) processes, Production Part Approval Process (PPAP), product qualification, validation, and supplier quality activities.
• Working knowledge of U.S. Food and Drug Administration (FDA) regulations and International Organization for Standardization (ISO) standards applicable to medical devices.
• Experience with metrology, Geometric Dimensioning and Tolerancing (GD&T), measurement uncertainty, Gauge Repeatability and Reproducibility (Gauge R&R), statistical analysis, and Minitab.
• Experience with Windchill or Agile Product Lifecycle Management (PLM) systems.
• American Society for Quality (ASQ) certification such as Certified Quality Engineer (CQE), Certified Quality Auditor (CQA), or Certified Supplier Quality Professional (CSQP), or Six Sigma, Design for Six Sigma (DFSS), Lean Green Belt, or Black Belt 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.

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.

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.

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.

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.

Salary ranges for U.S (excl. PR) locations (USD):$99,200.00 - $148,800.00

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

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.

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.