Senior Supplier Quality Engineer

We anticipate the application window for this opening will close on - 27 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.
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• Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses.
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• 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 .
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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.

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