Senior Supplier Quality Engineer

Regulatory Jobs; Grand Rapids (MI); On-site; USD 99,000 - 149,000; Full time

Job summary

Medtronic is seeking a Senior Supplier Quality Engineer for our Grand Rapids, MI site. The role focuses on supplier quality management for materials and components used in manufacturing, with emphasis on investigations, CAPAs, and supplier controls.

You will collaborate with engineering to define acceptance strategies, manage supplier onboarding, and ensure compliance with quality systems and regulatory requirements. This position requires onsite work five days a week with limited travel.

Qualifications

• Bachelor’s degree in Engineering/Science or technical field with 4+ years in Eng/Quality OR Advanced Degree with 2+ years in Eng/Quality OR PhD with 0 years relevant experience.
• ASQ Certified Quality Auditor or ASQ Lead Auditor certification.
• Experience with supplier quality in medical devices or other regulated manufacturing environments.

Responsibilities

• Manage supplier quality performance and monitor supplier compliance with quality requirements for materials, components, and services.
• Lead investigations related to supplier quality issues, nonconforming materials, CAPAs, MRB activities, and inspection findings.
• Coordinate supplier onboarding activities, including ASL additions and supplier setup across quality systems.
• Partner with engineering to develop product acceptance strategies and supplier control plans.
• Define receiving inspection requirements and support validation of internal test methods for supplied products.
• Evaluate supplier change notifications and assess impacts on manufacturing and inventory.
• Apply statistical quality techniques to analyze supplier performance and trends.
• Drive Lean, Six Sigma, Kaizen and other quality improvement initiatives.

Skills

Quality engineering

Data analysis

Problem solving

Education

Bachelor’s Degree in Engineering/Science/Technical field

Advanced Degree in Engineering/Science

PhD

Tools

Microsoft Word

Excel

PowerPoint

Project

Job description

We anticipate the application window for this opening will close on - 5 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 Grand Rapids, Michigan manufacturing site produces approximately 600 finished products, including cannulae and beating heart products used across Medtronic’s cardiovascular portfolio. The Supplier Quality Engineering function partners closely with suppliers and cross-functional teams to ensure purchased materials, components, and finished devices meet quality, regulatory, and operational requirements throughout the product lifecycle.

This position is based in Grand Rapids, MI and requires onsite work five (5) days per week to support supplier quality activities, manufacturing operations, and cross-functional collaboration. This role has minimal travel.

As a Senior Supplier Quality Engineer, you will support supplier quality management activities for purchased materials and components used in manufacturing. This role is responsible for supplier performance oversight, investigation of supplier-related quality issues, implementation of supplier controls, and support of product and process changes to ensure compliance with quality system and regulatory requirements.

Primary Responsibilities:

• Manage supplier quality performance and monitor supplier compliance with quality requirements for materials, components, and services.
• Lead investigations related to supplier quality issues, nonconforming materials, Supplier Corrective and Preventive Actions (CAPAs), Material Review Board activities, and inspection findings.
• Coordinate supplier onboarding activities, including Approved Supplier List (ASL) additions and supplier setup across applicable quality and business systems.
• Partner with engineering and cross-functional teams to develop product acceptance strategies, supplier control plans, and quality requirements for new products and processes.
• Define receiving inspection requirements and support validation of internal test methods associated with supplied products.
• Evaluate supplier change notifications and assess potential impacts to manufacturing operations, inventory, acceptance activities, and product configurations.
• Apply statistical quality techniques to analyze supplier performance, identify trends, and implement corrective actions.
• Drive continuous improvement initiatives using Lean, Six Sigma, Kaizen, and other quality improvement methodologies.

Required Qualifications:

• Requires a Bachelor’s Degree in Engineering, Science or technical field with 4+ years of work experience in Engineering and/or Quality OR Advanced Degree in Engineering, Science or technical field with 2+ years of work experience in Engineering and/or Quality OR PhD with 0 years relevant experience.

Preferred Qualifications:

• Experience investigating quality issues, nonconforming products, corrective actions, or supplier-related quality concerns.
• Knowledge of quality systems, regulated manufacturing environments, or supplier quality processes.
• Ability to analyze data and apply problem-solving methodologies to support quality and process improvements.
• Experience in supplier quality engineering within the medical device industry or another regulated manufacturing environment.
• Working knowledge of Quality System Regulation (21 CFR Part 820), ISO 13485, statistical quality control methods, and Six Sigma principles.
• Experience with supplier controls, process validation, auditing, failure investigations, nonconforming product management, and protocol or report development.
• ASQ Certified Quality Auditor or ASQ Lead Auditor certification.
• Proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, and Project.

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 - $148,800.00This 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 pertain 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, andSimple 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), andCapital 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.