Medtronic

Supplier Quality Engineer II

Medtronic$80K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Engineering, Science, or technical field with 2+ years in Engineering/Quality, or Advanced Degree with 0+ years experience.
  • Proven experience in supplier quality management within the medical device industry.
  • Strong knowledge of Quality System Regulation, ISO 13485, and statistical quality control methods.
  • ASQ Lead Auditor certification preferred.
  • Excellent communication skills for cross-level collaboration.

Responsibilities

  • Ensure suppliers deliver quality parts, materials, and services.
  • Conduct investigations into supplier quality issues; lead MRB and Nonconformance activities.
  • Manage Supplier/Part Setup in multiple applications.
  • Coordinate changes of New Suppliers to the Approved Supplier List.
  • Collaborate with engineers to develop Product Acceptance Strategies and Quality controls for new products.
  • Define Receiving Inspection requirements and test method validations.
  • Support supplier change notices and assess impact on manufacturing operations.
  • Utilize statistics to monitor supplier quality issues and drive continuous improvement.

Benefits

  • Health, Dental, and Vision insurance.
  • Health Savings Account and Healthcare Flexible Spending Account.
  • Life insurance and Long-term disability leave.
  • Tuition assistance and reimbursement.
  • 401(k) plan with employer match.
Full Job Description
We anticipate the application window for this opening will close on - 4 Aug 2026

A Day in the Life

The Medtronic Mindset challenges us to act boldly, move with urgency, collaborate effectively, and deliver results-the right way. At Medtronic, our most impactful technical leaders bring deep expertise, strong influence, and the ability to drive meaningful improvements across complex supplier networks.

In this exciting role as a Supplier Quality Engineer II, you will have responsibility for management of suppliers within the at our Grand Rapids, MI manufacturing team. You will be accountable for changes to existing supplied products and processes, as well as oversight of performance and improvement activities. The Grand Rapids site manufactures approximately 600 finished products, including cannulae and beating heart products.

You will also lead the oversight of supplied products, ensuring conformance to purchased materials or finished devices requirements and management of nonconforming product in compliance to Medtronic Purchasing and Supplier Controls, FDA, and international requirements and Quality System Regulations.

At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We're working a minimum of 5 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.

Responsibilities may include the following and other duties may be assigned.
  • Ensure that suppliers deliver quality parts, materials, and services.
  • Perform timely investigations into supplier quality issues. Lead activities related to Material Review Board (MRB), Nonconformance's (NCMR), Supplier CAPAs and Inspections.
  • Responsible for Supplier/Part Setup and Management in multiple applications.
  • Coordinate the addition/change of New Suppliers to the Approved Supplier List (ASL).
  • Collaborate with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products.
  • Define Receiving Inspection requirements as required and associated test method validation for all internal Medtronic Test Methods.
  • Support supplier change notices and assess their impact to MTC manufacturing operations, to existing material inventory, to acceptance procedures and part number configurations.
  • Stay abreast of applicable regulatory requirements. Actively seek out opportunities to understand current industry direction.
  • Apply understanding of statistical concepts to monitor suppliers and correct supplier quality issues.
  • Drive continuous improvement using such tools as Lean, Six Sigma and Kaizen. All activities must be performed in compliance with the Quality System.


Must Have: Minimum Requirements
  • Requires a 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.


Nice to Have
  • Proven supplier quality engineering experience within the medical device industry (or related regulated industry), including expertise in supplier quality management, supplier controls, process validation, auditing, failure investigations, nonconforming product controls, and protocol/report preparation.
  • Strong working knowledge of Quality System Regulation (21 CFR Part 820), ISO 13485, statistical quality control methods, and Six Sigma principles.
  • ASQ Lead Auditor certification preferred.
  • Excellent written and verbal communication skills, with the ability to build and maintain professional, collaborative relationships across all levels of the organization.
  • Proficient in 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. a7 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.

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 [redacted].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 [redacted].

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):$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

About Medtronic

Medtronic plc is an Irish-domiciled multinational medical device company that develops and manufactures medical device technologies and therapies to treat chronic diseases worldwide. Medtronic was founded in 1949 in Minneapolis, Minnesota, as a medical equipment repair shop. Today, the company operates in more than 160 countries and employs over 90,000 people. Medtronic's primary products include implantable pacemakers and defibrillators, insulin pumps, spinal and neurostimulation devices, surgical tools, and patient monitoring systems. The company is committed to improving patient outcomes and expanding access to healthcare through innovative medical technologies.
Learn more about Medtronic
Size
95,000 employees
Market Cap
$102.7 billion
Industry
Net Income
$2.8 billion
Founded
1949
5 Year Trend
+1.3%
Revenue
$27.9 billion
NASDAQ

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