À propos de ce poste Supplier Quality Engineer II chez Medtronic
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 Peripheral Vascular Health portfolio develops and manufactures technologies used to treat vascular disease, including peripheral stents and delivery systems. The Nathan Lane manufacturing site in Plymouth, Minnesota supports approximately 20 product families and works closely with suppliers to ensure the quality, reliability, and compliance of components used throughout the portfolio.This position is part of the Supplier Quality organization and partners with engineering, operations, and global quality teams to improve supplier performance, address quality risks, and support a stable supply chain. This is an onsite position based in Plymouth, Minnesota with an expectation of working onsite five days per week. Travel is expected to be 10% or less.
As a Supplier Quality Engineer II, you will serve as a technical resource for supplier quality activities supporting the Nathan Lane manufacturing site. This role is responsible for resolving supplier quality issues, driving performance improvements across the supply base, and partnering with internal and external stakeholders to ensure compliant and effective quality systems.
Primary Responsibilities
Lead investigations and resolution of supplier quality issues that impact product quality, manufacturing performance, or compliance requirements.
Partner with suppliers to identify root causes, implement corrective and preventive actions, and verify effectiveness of improvements.
Analyze supplier performance data and develop strategies to improve supplier quality, delivery performance, and process capability.
Collaborate with engineering, operations, and quality teams to assess supplier-related risks and implement sustainable solutions.
Support supplier qualification, change management, and ongoing supplier monitoring activities.
Conduct supplier audits and evaluate supplier quality systems against applicable regulatory and company requirements.
Drive continuous improvement initiatives focused on defect reduction, issue prevention, and supplier quality performance.
Provide technical guidance and influence cross-functional teams on supplier quality strategies and decisions.
Required Qualifications
Bachelor's degree and 2+ years of relevant experience in supplier quality, quality engineering, manufacturing engineering, or a related engineering discipline; OR Advanced Degree and 0+ years of relevant experience.
Preferred Qualifications
Experience in the medical device industry or another highly regulated manufacturing environment, including supplier quality management, supplier controls, process validation, supplier auditing, failure investigations, nonconforming product controls, and technical documentation development.
Working knowledge of Quality System Regulation (21 CFR Part 820), ISO 13485, corrective and preventive action (CAPA), risk management, change control, and supplier quality system requirements.
Experience applying quality engineering tools and methodologies, including Failure Modes and Effects Analysis (FMEA), statistical quality control, process capability analysis, and Six Sigma principles.
Professional quality certifications such as ASQ Certified Quality Engineer (CQE) or ASQ Lead Auditor certification.
Strong communication and collaboration skills with experience influencing suppliers and cross-functional stakeholders; proficiency with Microsoft Office applications including Excel, Word, 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.
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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 [email protected].
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.
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.