Medtronic

Test Engineer I

Medtronic$70K — $105K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a technically related field (STEM)
  • Experience with medical device testing and understanding of FDA Quality System Regulations (QSR)
  • Working knowledge of software design, development, debug and test practices
  • Familiarity with generative AI tools (e.g., ChatGPT, Copilot)
  • Experience with test automation including GUI, integration, and stress testing.

Responsibilities

  • Design, develop, and implement testing methods and equipment for medical products.
  • Compile data and suggest improvements for testing procedures and equipment.
  • Perform verification and validation of products through generated plans and protocols.
  • Create and maintain test software to support product verification.
  • Ensure test equipment is operational and calibrated for reliability.

Benefits

  • Health, Dental, and Vision insurance
  • Tuition assistance/reimbursement
  • 401(k) plan with employer contribution
  • Paid time off and paid holidays
  • Employee Stock Purchase Plan
Full Job Description
We anticipate the application window for this opening will close on - 22 Jun 2026

A Day in the Life

Across our global Neuroscience organization, we advance care for some of medicine's most complex neurological and spinal conditions. By combining innovative technology, data-driven insights, and deep clinical expertise, we partner with physicians and health systems to improve how patients are treated and supported throughout their care journey.

Our Cranial & Spinal Technologies (CST) Operating Unit develops and delivers an integrated ecosystem of spinal implants, navigation and robotic guidance systems, advanced imaging, and data-driven planning tools for complex spine and cranial procedures. Platforms such as AiBLE™ connect these technologies to enhance surgical precision, streamline workflows, and support improved patient outcomes across the globe.

The Test Engineer I has the responsibility and authority to design, develop, and implement testing methods and equipment to ensure Medtronic's cutting edge medical products meet our user's needs and our quality and reliability standards. The Test Engineer I performs verification testing of mechanical, electro-mechanical and software products for compliance, accuracy and reliability. Work is performed under leadership direction.

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 10 - 20% of travel to enhance collaboration and ensure successful completion of projects.

Responsibilities:
  • Responsible for plans, schedules and equipment required for testing including tool/fixture/phantom design.
  • Compiles data and defines changes required in test equipment, testing procedures, manufacturing processes, or new testing requirements.
  • Frequent use and application of technical standards, principles, theories, concepts, and techniques.
  • Responsible for verification and validation of new or changed products including generating plans, protocols and reports for testing performed.
  • Create, develop and maintain test software.
  • Ensures test equipment is in good working order and calibrated, as necessary.
  • Coordinates and oversees the testing of equipment and product at outside test facilities.
  • Sets up and develops test tracking, monitoring and data recording systems.
  • Provides solutions to a variety of technical problems of moderate scope and complexity.
  • Participate in all phases of product development as needed such as reviewing requirements, design, usability, risk assessment and defects.
  • Design, implement and/or execute automated testing.
  • Identify and implement process improvements.
  • Participate in defect tracking and analysis.
  • Troubleshoot, debug, maintain, and support existing products.
  • Effectively communicate findings, problems and solutions to project teams and stakeholders.
  • Collaborate and maintain excellent working relationships with team members and stakeholders.
  • All activities must be performed in compliance with the Quality System.
  • Performs duties in compliance with environmental, health and safety related site rules, policies or governmental regulations.
  • All other duties as assigned.


Must Have: Minimum Requirements:
  • Bachelor's degree in a technically related field (STEM)


Nice to Have:
  • Working knowledge of software design, development, debug and test practices.
  • Oral and written communication skills.
  • Ability to work in a team environment.
  • Willingness to learn and apply generative AI tools (e.g., ChatGPT, Copilot) to improve work efficiency, including writing and debugging scripts, analyzing code or requirement changes, and streamlining documentation tasks.


  • Experience with medical device testing and understanding of FDA Quality System Regulations (QSR)
  • Familiarity with generative AI tools (e.g., ChatGPT, Copilot) to writing and debugging scripts
  • Experience with test automation including GUI, integration and stress testing and designing and implementing test automation frameworks.
  • Experience with utilizing AI for
  • Able to handle multiple tasks/projects and manage priorities
  • Ability to work in a fast paced, collaborative team environment. Experience with Agile and iterative development practices is a plus.
  • Project management skills including planning, estimation, tracking and communication
  • Self-motivated with strong problem-solving skills and the ability to work independently
  • Experience with C++, Linux, Python, Perl, SQL, XML, Selenium, Javascript, continuous integration and other technical tools.
  • Machine shop experience.
  • Knowledge of statistical methods.

For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. A7 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.

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 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):$70,400.00 - $105,600.00

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 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

About Medtronic

Medtronic plc is an Irish-domiciled multinational medical device company that develops and manufactures medical device technologies and therapies to treat chronic diseases worldwide. Medtronic was founded in 1949 in Minneapolis, Minnesota, as a medical equipment repair shop. Today, the company operates in more than 160 countries and employs over 90,000 people. Medtronic's primary products include implantable pacemakers and defibrillators, insulin pumps, spinal and neurostimulation devices, surgical tools, and patient monitoring systems. The company is committed to improving patient outcomes and expanding access to healthcare through innovative medical technologies.
Learn more about Medtronic
Size
95,000 employees
Market Cap
$102.7 billion
Industry
Net Income
$2.8 billion
Founded
1949
5 Year Trend
+1.3%
Revenue
$27.9 billion
NASDAQ

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