Prin. Test Engineer - Onsite

Medtronic plc; United States; Sur place; USD 129 000 - 193 000; Plein temps

Avantages offerts par ce poste

Health, Dental and vision insurance

401(k) with employer match

Tuition assistance

Résumé du poste

Medtronic plc in Colorado seeks a Principal Test Engineer to lead system-level verification and validation for interventional medical devices from concept to commercialization. You will develop robust test strategies, write verification and validation plans, and drive regulatory-ready documentation with cross-functional partners.

Based in Lafayette, CO, this onsite role requires technical leadership, mentorship of engineers, and collaboration with quality, manufacturing, and regulatory teams to

Qualifications

• Bachelor's degree with 7+ years of engineering or technical testing experience; or Master's with 5+ years; or PhD with 3+ years.
• Experience leading system-level verification/validation planning, execution, and documentation.
• Experience developing test methods, verification protocols, acceptance criteria, and reports.
• Strong knowledge of mechanical and electrical engineering fundamentals and related test equipment.
• Experience collaborating across cross-functional product development teams.

Responsabilités

• Lead system-level verification and validation strategy, planning, execution, and reporting for new product development programs.
• Develop verification protocols, including acceptance criteria, statistical rationale, and sample size justifications.
• Design, validate, and implement test methods to evaluate system compatibility, reliability, mechanical performance, electrical performance, and tissue interaction.
• Generate regulatory submission-ready documentation, including verification reports, validation reports, and verification traceability evidence.
• Lead user needs validation activities in real or simulated use environments and document objective evidence of design effectiveness.
• Facilitate design reviews, risk management activities, and cross-functional decision-making throughout the product development lifecycle.
• Partner with systems, quality, manufacturing, regulatory, marketing, human factors, and engineering teams to ensure compliance with applicable medical device requirements and standards.
• Provide technical leadership and mentorship to engineers, laboratory personnel, and external development partners.

Connaissances

System-level V&V

Test method design

Regulatory documentation

Cross-functional teamwork

Mechanical & electrical fundamentals

Formation

Bachelor's degree in engineering

Master's degree

PhD

Outils

Test equipment

Description du poste

We anticipate the application window for this opening will close on - 26 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 Life At Medtronic Neuroscience

we bring innovation, expertise, and purpose together to improve outcomes and transform lives for people living with neurological, spine, and chronic pain conditions. Medtronic Neuromodulation advances innovative therapies that restore function and relieve chronic pain. We help patients reclaim their lives and achieve better outcomes.

Check us out on LinkedIn: Medtronic Brain Modulation and Pain Interventions

As a Test Engineer within the Neuromodulation Interventional organization, you will utilize your expertise in test and engineering to delivering cutting edge products that focus on ablating tumors in patients. Medtronic has been shaping the approach to minimally invasive tumor treatment for over 25 years and is redefining standard of care for metastatic cancer in the liver with the revolutionary EmprintTM microwave ablation system with ThermosphereTM technology. The Medtronic Interventional team also invented the first balloon kyphoplasty devices for the treatment of vertebral compression fractures and continue to deliver breakthrough innovative RF ablation systems to treat metastatic and benign spinal tumors and alleviate chronic pain through targeted nerve ablation. This position is based in Lafayette, Colorado and requires onsite presence. As a Principal Test Engineer, you will lead system-level verification and validation strategy for interventional medical devices from concept through commercialization. You will drive the development of robust test methods, verification plans, validation activities, and regulatory-ready documentation while providing technical leadership across multidisciplinary product development teams.

Primary Responsibilities

Lead system-level verification and validation strategy, planning, execution, and reporting for new product development programs. Develop verification protocols, including acceptance criteria, statistical rationale, and sample size justifications. Design, validate, and implement test methods to evaluate system compatibility, reliability, mechanical performance, electrical performance, and tissue interaction. Generate regulatory submission-ready documentation, including verification reports, validation reports, and verification traceability evidence. Lead user needs validation activities in real or simulated use environments and document objective evidence of design effectiveness. Facilitate design reviews, risk management activities, and cross-functional decision-making throughout the product development lifecycle. Partner with systems, quality, manufacturing, regulatory, marketing, human factors, and engineering teams to ensure compliance with applicable medical device requirements and standards. Provide technical leadership and mentorship to engineers, laboratory personnel, and external development partners.

Required Qualifications

Bachelor's degree with 7+ years of engineering or technical testing experience OR Master's degree with 5+ years of engineering or technical testing experience OR PhD with 3+ years of engineering or technical testing experience. Experience leading system-level verification and/or validation planning, execution, and documentation for complex products. Experience developing test methods, verification protocols, acceptance criteria, and technical reports. Knowledge of mechanical and electrical engineering fundamentals and associated test equipment. Experience working effectively across cross-functional product development teams.

Preferred Qualifications

Experience in regulated industries such as medical device, aerospace, or defense. Experience testing medical devices or systems in ex-vivo tissue environments. Knowledge of IEC 60601 standards, electrical safety testing, and electromagnetic compatibility (EMC) testing. Experience with system-level requirements traceability from design inputs through verification evidence. Experience supporting products with integrated mechanical, electrical, and software subsystems across the full V-model 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 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.

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):$128,800.00 - $193,200.00

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 plans

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.

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 settingis 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. This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here.

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