Quality Engineering Senior
$99.2k - $148.8kMedtronic
Remote
Full time
We anticipate the application window for this opening will close on - 29 Sep 2026
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.
The Supplier Quality function partners with Contract Manufacturers (CMs), Original Equipment Manufacturers (OEMs), and critical suppliers to ensure the quality, compliance, and performance of externally manufactured products and components. This team works cross-functionally with Research & Development (R&D), Quality, Regulatory Affairs, and Operations to support product lifecycle activities, drive supplier performance improvements, and maintain compliance with applicable quality system and regulatory requirements.
This position may be performed remotely anywhere within the United States. Travel up to 15% is required to support supplier audits, supplier performance reviews, business meetings, and cross-functional initiatives.
The Senior Supplier Quality Engineer serves as the primary quality partner for strategic Contract Manufacturers and Original Equipment Manufacturers, ensuring supplier processes, products, and quality systems consistently meet Medtronic requirements. This role drives supplier quality performance, supports product and process changes, leads quality improvement initiatives, and provides technical quality guidance across supplier-related activities throughout the product lifecycle.
Manage quality oversight of strategic Contract Manufacturers (CMs), Original Equipment Manufacturers (OEMs), and designated suppliers to ensure compliance with product, process, and quality system requirements.
Lead supplier quality activities associated with product and process changes, including risk assessment, qualification, validation, and implementation support.
Monitor supplier performance metrics, identify quality risks and trends, and drive corrective and preventive actions to improve supplier effectiveness and product quality.
Plan, conduct, and support supplier audits to assess compliance with Good Manufacturing Practices (GMP), quality standards, and regulatory requirements.
Partner with Research & Development (R&D), Regulatory Affairs, Operations, and Quality teams to ensure supplied products and components meet finished device requirements.
Investigate supplier-related nonconformances, complaints, and quality issues, facilitating root cause analysis and sustainable corrective actions.
Provide Supplier Quality support for New Product Development (NPD) activities, including supplier qualification, product acceptance strategies, control plans, and supplier quality deliverables.
Define and maintain receiving inspection requirements, supplier controls, and quality documentation necessary to support product acceptance and compliance.
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.
Experience working with supplier quality systems, supplier qualification, supplier audits, or supplier performance management.
Experience supporting quality processes within a regulated industry environment.
Experience interpreting and applying quality system requirements, technical documentation, specifications, and quality standards.
Experience supporting Contract Manufacturers (CMs), Original Equipment Manufacturers (OEMs), or external manufacturing partners within the medical device industry.
Lead Auditor or certified quality-related credential such as American Society for Quality (ASQ) certification.
Knowledge of ISO 13485, 21 CFR Part 820, Good Manufacturing Practices (GMP), and global medical device regulatory requirements.
Experience leading supplier corrective actions, continuous improvement initiatives, and cross-functional quality projects.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: 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.
In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) Recruitment Fraud Alert
All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.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. 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 View email address on click.appcast.io offers a competitive Salary and flexible Benefits Package
They share in the success they help to create. 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).
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).
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).
Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. 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.
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. Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
With one Medtronic Mindset defining how we work. Build a better future, amplifying your impact on the causes that matter to you and the world
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.
We advance healthcare, society, and equity with every design, inside and outside our walls.
Insight-driven care . 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 setting?is 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.
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email View email address on click.appcast.io request removal of your personal information from our systems please email View email address on click.appcast.io.
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