Senior Research & Development Test Engineer - Onsite

Medtronic; Santa Clara (CA); On-site; USD 115,000 - 173,000; Full time

Benefits offered by this job

Health, Dental and Vision Insurance

401(k) with employer match

Tuition assistance

Flexible Spending Accounts

Job summary

Medtronic in Santa Clara, California, seeks a Research & Development Test Engineer to lead system-level verification and validation activities for interventional pain therapies and related medical device systems. You will craft test strategies, run protocols, analyze results, and document findings while partnering with systems engineering, quality, regulatory, and manufacturing teams.

Required 4+ years in technical testing, verification, and validation, plus experience with medical devices or

Qualifications

• Bachelor's degree in Engineering or a scientific discipline and 4+ years of technical testing, verification, and validation.
• Experience leading system-level verification planning and documentation.
• Experience leading system-level validation planning and documentation.
• Experience testing medical devices or ex-vivo tissues.
• Knowledge of IEC 60601 standards and regulatory basics is preferred.

Responsibilities

• Develop and execute system-level verification strategies for medical device systems containing mechanical, electrical, and software components.
• Create test methods, protocols, validation plans, and reports to support product development.
• Plan and perform verification and validation testing with risk assessment and documentation.
• Collaborate with cross-functional teams to establish test requirements and inputs.
• Lead design reviews and support risk management through the lifecycle.

Skills

System verification

System validation

Medical device testing

Electrical test tools

Education

Bachelor's degree in Engineering or science

Tools

Oscilloscopes

Multimeters

Job description

We anticipate the application window for this opening will close on - 5 Sep 2026Careers 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 LifeThe Neuromodulation Research & Development organization develops therapies and technologies that address chronic pain and other neurological conditions. Within the Interventional Pain portfolio, teams focus on minimally invasive therapies used to treat musculoskeletal pathologies, including vertebral compression fractures, nerve pain, metastatic bone tumors, and benign bone tumors. This role supports the development of system-level verification and validation strategies for new products and enhancements across mechanical, electrical, and software components.This position is based in Santa Clara, California, and follows an onsite work model. No travel is required for this role.As a Research & Development Test Engineer, you will lead and execute verification and validation activities that support the development of interventional pain therapies and associated medical device systems. You will collaborate with cross-functional partners to define test strategies, evaluate product performance, manage technical risks, and generate evidence needed to support product development and regulatory requirements.Primary ResponsibilitiesDevelop and execute system-level verification and validation strategies for medical device systems containing mechanical, electrical, and software components.Create test methods, test protocols, test method validation plans, and engineering reports to support product development activities.Plan and perform verification and validation testing, including analysis of results, risk assessment, and documentation of findings.Partner with systems engineering, quality, manufacturing, regulatory, human factors, and marketing teams to establish test requirements and design inputs.Lead design review activities and support risk management processes throughout the product development lifecycle.Conduct testing and validation activities in simulated-use environments and with representative end users when required.Perform testing of minimally invasive therapy products and procedures in accordance with applicable standards, procedures, and quality requirements.Communicate technical findings, recommendations, and project status to stakeholders and provide technical guidance to internal team members and external development partners.Required QualificationsBachelor's degree in Engineering or a scientific discipline and 4+ years of technical testing, verification, and validation, systems engineering, or product development experience.Experience leading system-level verification planning, execution, and documentation for complex products or systems.Experience leading system-level validation planning, execution, and documentation.Experience testing medical devices or similar products in ex-vivo tissue environments.Working knowledge of software development principles, electrical engineering fundamentals, and electrical test equipment such as oscilloscopes and multimeters.Preferred QualificationsExperience working 3-8 years testing in regulated industries such as medical device, aerospace, or defense.Knowledge of IEC 60601 standards, electrical safety testing, and electromagnetic compatibility (EMC) testing.Experience performing requirements traceability from system design inputs through verification and validation results.Experience supporting products that integrate mechanical, electrical, and software subsystems.Experience leading systems engineering activities across the full V-model product development lifecycle.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 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 & SponsorshipAt 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 AlertWe 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 [e-mail] .Benefits & CompensationMedtronic 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 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):$115,200.00 - $172,800.00This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).The base salary range applies across the United States, excluding Puerto Rico and certain 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 plansIt 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.