Senior Supplier Quality Engineer

Medtronic; Warszawa; On-site; PLN 388,000 - 582,000; Full time

Benefits offered by this job

Health insurance

401(k) plan with match

Tuition assistance

Job summary

Medtronic is seeking an on-site Senior Supplier Quality Engineer in Memphis, TN, to lead supplier quality activities for additive manufacturing, including qualification, validation, and continuous improvement. This role requires collaboration with suppliers and cross-functional teams and up to 25% travel to supplier and business locations.

You will ensure AM processes, materials, equipment, and controls meet quality and regulatory requirements, supporting supplier selection, qualification, and

Qualifications

• Bachelor's degree with 4+ years of relevant experience, or Master's with 2+ years, or PhD with 0 years.
• 2+ years of supplier quality or related quality-focused role in regulated environments.

Responsibilities

• Assess and qualify additive manufacturing suppliers through technical evaluations and quality system assessments.
• Lead supplier audits to verify GMP and industry standards compliance.
• Evaluate AM process capability, validation strategies, and manufacturing controls.
• Support PPAP, supplier qualification, and validation for new and existing suppliers.
• Investigate supplier quality issues, identify root causes, and implement corrective actions.
• Partner with NPD, Component Engineering, and Supplier Quality teams across the product lifecycle.
• Develop risk-based supplier quality strategies for AM processes, materials, and technologies.
• Define receiving inspection requirements, test methods, and quality controls.

Skills

Supplier quality

Quality engineering

Audits

Education

Bachelor's degree in related field

Master's degree in related field

Job description

Onsite

Memphis, Tennessee, United States of America

Fridley, Minnesota, United States of America

Warsaw, Indiana, United States of America

Full time

R75723

We anticipate the application window for this opening will close on - 14 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.

A Day in the Life

The Supplier Quality function partners with external suppliers to ensure purchased materials, components, and services meet quality, regulatory, and business requirements throughout the product lifecycle. This team drives supplier qualification, process validation, risk management, and continuous improvement activities to support product quality and business objectives across advanced manufacturing technologies.

This position is based onsite in Memphis, Tennessee. The role requires collaboration with suppliers and cross-functional teams and includes up to 25% travel to supplier and business locations.

The Supplier Quality function partners with external suppliers to ensure purchased materials, components, and services meet quality, regulatory, and business requirements throughout the product lifecycle. This role provides specialized Supplier Quality Engineering expertise in additive manufacturing (AM), supporting supplier qualification, process validation, risk assessment, and continuous improvement activities for advanced manufacturing technologies.

As a Senior Supplier Quality Engineer, you will serve as a technical subject matter expert for additive manufacturing supplier quality. You will support supplier selection, qualification, validation, and performance management activities while helping ensure additive manufacturing processes, materials, equipment, and controls meet quality and regulatory requirements. This role partners closely with suppliers and internal stakeholders to identify risks, drive process improvements, and support the delivery of high-quality products and components.

Primary Responsibilities

• Assess and qualify additive manufacturing suppliers through technical evaluations, process reviews, and quality system assessments.

• Lead supplier audits and oversight activities to verify compliance with quality requirements, Good Manufacturing Practices (GMP), and applicable industry standards.

• Evaluate additive manufacturing process capability, validation strategies, and manufacturing controls to ensure consistent product quality.

• Support Production Part Approval Process (PPAP), supplier qualification, and validation activities for new and existing suppliers.

• Investigate supplier quality issues, identify root causes, implement corrective actions, and monitor effectiveness of improvements.

• Partner with New Product Development, Component Engineering, and Supplier Quality teams to support supplier engagement throughout the product lifecycle.

• Develop and implement risk-based supplier quality strategies for additive manufacturing processes, materials, and technologies.

• Define receiving inspection requirements, test methods, and quality controls to support product acceptance and supplier performance objectives.

Required Qualifications

• Bachelor's degree and 4+ years of relevant experience, OR Master's degree and 2+ years of relevant experience, OR PhD with 0 years of relevant experience.

• 2+ years of experience in supplier quality, quality engineering, manufacturing engineering, or a related quality-focused role supporting regulated manufacturing environments.

Preferred Qualifications

• Experience supporting additive manufacturing technologies, processes, materials, equipment, or supplier networks.

• Experience conducting supplier assessments, supplier qualification activities, audits, or quality system evaluations.

• Experience with Production Part Approval Process (PPAP), process validation, manufacturing process controls, corrective and preventive actions (CAPA), or continuous improvement initiatives.

• Knowledge of quality management systems, supplier quality requirements, and risk management principles within regulated industries.

• ASQ Certified Quality Engineer (CQE), Certified Supplier Quality Professional (CSQP), or similar quality 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 (https://www3.benefitsolver.com/benefits/BenefitSolverView?page_name=signon&co_num=30601&co_affid=medtronic)

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 (https://www.medtronic.com/content/dam/medtronic-wide/public/united-states/employee-support-services/careers/la-county-legal-notice.pdf) 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.

We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.

Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.

We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.

We change lives

Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That’s who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.

We build extraordinary solutions as one team

With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.

This life-changing career is yours to engineer

By bringing your ambitious ideas, unique perspective and contributions, you will…

• Build a better future, amplifying your impact on the causes that matter to you and the world

• Grow a career reflective of your passion and abilities

• Connect to a dynamic and inclusive culture that welcomes the challenge of life-long learning

These commitments set our team apart from the rest:

Experiences that put people first

Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.

Life-transforming technologies

No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.

Better outcomes for our world

Here, it’s about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.

Insight-driven care

Fresh viewpoints. Cutting-edge AI, data, and automation. You’re shaping the future of healthcare technology and defining the next generation of breakthroughs in care

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.

For sales reps and other patient facing field employees, going into a healthcare settingis considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.

This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here (https://www.e-verify.gov/employees) .