R&D Engineer I

Job description

We anticipate the application window for this opening will close on - 11 Aug 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 LifeMedtronic’s Interventional Cardiology Therapies R&D group is looking for a motivated engineer to be part of a high-performing team that is revolutionizing the design and development of medical devices. In this role, you will leverage both your technical breadth and business acumen to maintain the design integrity of commercially available products. The work you do will impact patients globally and help support Medtronic’s mission of alleviating pain, restoring health, and extending life for millions. This position requires strong technical skills to support commercial product continuity and our global supply of products designed to treat diseases of the vascular system. The R&D Engineer will apply advanced engineering principles, theories, and concepts in working on complex technical problems and will provide technical support on post market objectives. 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 are working onsite a minimum of 4 days per week as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. This role will require less than 10% of travel to enhance collaboration and ensure successful completion of projects. Responsibilities may include the following, and other duties may be assigned: Work in Released Product Engineering for root cause investigations, complaints analysis, manufacturing process changes, supplier change notifications and implementing corrective and preventive measures Develop design concepts/prototypes/test methodology to conduct material, component, and device level testing to meet development and regulatory requirements Conduct design verification and validation testing per approved protocols and document in accordance with applicable development regulatory requirements Prepare reports and presentations to communicate technical assessments and analysis results Maintain product design integrity of commercially available products using sound engineering principles while working within appropriate Design Control requirements Apply problem solving skills, critical thinking, technical principles, and theories to solve complex problems in the field of structural heart disease treatment Investigate product design and reliability issues in partnership with other R&D Engineers, Manufacturing Engineers, Quality Engineers, and other cross-functional departments to determine root cause and implement solutions Review and approve change orders of post-market products ensuring design integrity and reliability targets are met Review and approve design and process qualifications Review and approve verification and validation documentation Oversee process development objectives of internal and external partners Develop technical solutions and conduct testing, evaluate results using appropriate statistical analysis tools, and generate test reports Work collaboratively with external suppliers and business partners as well as internal cross-functional team members to maintain post market product quality Provide technical input supporting submissions to regulatory bodies and governmental agencies Support multiple projects within the Development group Desired/Preferred Qualifications High level proficiency of technical principles, theories, and design concepts in the field of medical device design and manufacturing Experience in Released Product Engineering Experience with Implant Design and Tissue processing Experience with Nitinol material and stent processing Experience with textile and suture development and testing a plus. Experience in design verification and validation. Experience with design and process qualification. Must Have: Minimum Requirements Requires a Baccalaureate degree and 0 years relevant experience 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):$74,400.00 - $111,600.00 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 fo