Supplier Quality Engineer II

Job description

We anticipate the application window for this opening will close on - 21 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 LifeThis role supports Supplier Quality within Medtronic, partnering with Contract Manufacturers (CMs), Original Equipment Manufacturers (OEMs), and sub-tier suppliers to ensure the quality, compliance, and continuous improvement of supplied medical devices and components. The team collaborates closely with Research & Development, Quality, Regulatory, and supplier partners to maintain effective quality systems, support product and process changes, and drive supplier performance across the product lifecycle. This is a U.S. Remote position. Candidates may be located anywhere within the United States but preference is the Midwest. Travel of up to 15% is required to support supplier visits, audits, business reviews, and cross-functional activities. The Supplier Quality Engineer II is responsible for managing supplier quality activities for Contract Manufacturers and Original Equipment Manufacturers, ensuring supplied products and processes meet Medtronic quality, regulatory, and customer requirements. This role partners with internal and external stakeholders to support product and process changes, monitor supplier performance, implement corrective actions, and drive continuous improvement across the supply base. Primary Responsibilities Manage supplier quality relationships with Contract Manufacturers (CMs), Original Equipment Manufacturers (OEMs), and sub-tier suppliers to ensure compliance with quality and regulatory requirements. Support supplier-related product and process changes through effective quality planning, risk assessment, validation, and change control activities. Monitor supplier quality performance using established metrics and lead improvement initiatives to address quality, delivery, and compliance concerns. Conduct supplier audits, assessments, and business reviews to evaluate quality system effectiveness and identify opportunities for improvement. Investigate quality issues, facilitate root cause analysis, and drive corrective and preventive actions with suppliers and internal stakeholders. Partner with Research & Development, Quality, Regulatory, Operations, and Manufacturing teams to ensure supplied products meet finished device requirements. Review and approve supplier quality documentation, including nonconformance investigations, corrective actions, process validations, and change notifications. Ensure supplier activities comply with applicable medical device regulations, industry standards, and internal quality system requirements. Required Qualifications 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 Experience working within the medical device, pharmaceutical, biotechnology, or other highly regulated industry. Preferred Qualifications Experience working with supplier quality systems, quality audits, corrective and preventive actions (CAPA), and change management processes. Experience supporting Contract Manufacturers (CMs), Original Equipment Manufacturers (OEMs), or external supplier networks. Experience supporting regulated products within a quality-controlled manufacturing environment. Knowledge of root cause analysis methodologies and continuous improvement tools. Knowledge of FDA Quality System Regulation (21 CFR Part 820), ISO 13485, and risk management principles. Experience conducting supplier audits and leading supplier quality improvement initiatives. Certification as a Quality Engineer, Auditor, or related quality professional 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. ‌ 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 @medtronic.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 AskHR@medtronic.com. ‌ 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 day