Reliability Engineer I – NV – Irvine, CA (Onsite)

We anticipate the application window for this opening will close on - 11 Jun 2026 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeAt 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 4 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.                  Our Neurovascular Operating Unit develops and delivers advanced, minimally invasive endovascular technologies for the treatment of acute ischemic and hemorrhagic stroke, brain aneurysms, and other complex cerebrovascular conditions. Through catheters, stent retrievers, flow diversion, and embolization systems, these solutions enable rapid, image-guided interventions that restore blood flow, secure vessels, and support consistent performance in high-acuity neurovascular procedures.Check us out on LinkedIn: Medtronic NeurovascularAs Reliability Engineer II, you ensure the performance, reliability, and safety of neurovascular products by designing and executing test plans, analyzing field and test data, and partnering with R&D, Clinical, Regulatory, and Manufacturing to mitigate risks across the product lifecycle. You will support root cause investigations, drive continuous improvement of reliability methods, and provide data-driven insights to inform design decisions in a highly regulated, cross-functional environment.Responsibilities may include the following and other duties may be assigned.Develops, coordinates, and conducts technical reliability studies and evaluations of engineering design concepts and design of experiments (DOE) constructs.Recommend design or test methods and statistical process control procedures for achieving required levels of product reliability.Completes risk analysis studies of new designs and processes.Compiles and analyzes performance reports and process control statistics; investigates and analyzes relevant variables potentially affecting product and processes.Ensures that corrective measures meet acceptable reliability standards.Analyzes preliminary plans and develops reliability engineering programs to achieve company, customer, and governmental agency reliability objectives.May develop mathematical models to identify units, batches, or processes posing excessive failure risks.As necessary, propose changes in design or formulation to improve system and/or process reliability.May determine units and/or batches requiring environmental testing and specifies minimum number of samples to obtain statistically valid data.Location: Irvine, CAOnsite: At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. We’re working onsite 4 days a week to drive performance, foster an environment of belonging, and collaborate to inspire as we engineer the extraordinary. This role will require Must Have (Minimum Requirements):To be considered for this role, please ensure the minimum requirements are evident on your resume.Bachelor’s degree in engineering or related discipline required with a minimum of 0 years’ relevant experience, OR  Nice to Have:Experience in neurovascular or vascular medical device developmentExperience supporting Class III medical devices within a regulated environmentExperience designing and executing reliability studies, including DOE and statistical analysis methodsWorking knowledge of risk management tools (e.g., FMEA, fault tree analysis) for product and process reliabilityProficiency in statistical process control (SPC), data analysis, and reliability modeling to assess performance and failure trendsFor 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 RequirementsThe 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. Join us in our mission to alleviate pain, restore health, and extend life—where your unique background and perspective are valued. Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits PackageA 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 off