Medtronic

Test Engineer II

Medtronic$84K — $127K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering or Computer Science and 2+ years of relevant experience, OR Master's degree, OR PhD.
  • Knowledge of medical device standards and regulations such as AAMI, ISO, FDA, and EN.
  • Working knowledge of software design, development, debugging, and testing practices.
  • Experience with verification and validation activities for software and/or system-level products.
  • Effective communication skills and ability to work collaboratively across teams.

Responsibilities

  • Develop verification and validation strategies, test plans, protocols, and reports for software and system products.
  • Design, implement, execute, and maintain automated and manual test solutions for product development.
  • Create, develop, and maintain test software, tools, and infrastructure.
  • Collaborate with teams to review product requirements and documentation, ensuring usability and risk assessments.
  • Analyze test results, document findings, and recommend product improvements.
  • Coordinate testing activities and maintain test equipment calibration.
  • Support defect tracking, troubleshooting, and root cause investigations for product issues.

Benefits

  • Health, dental, and vision insurance options.
  • Health Savings Account and flexible spending accounts.
  • Life insurance and long-term disability benefits.
  • Tuition assistance and reimbursement programs.
  • 401(k) plan with employer contributions and matches.
Full Job Description
We anticipate the application window for this opening will close on - 14 Sep 2026

A Day in the Life

The Neuroscience portfolio at Medtronic develops technologies that treat disorders and diseases affecting the brain, spine, and nervous system. Our teams combine clinical insight, engineering expertise, and advanced technologies to deliver therapies that help improve patient outcomes and quality of life around the world.

Within Cranial and Spinal Technologies (CST), we bring together technologies across Spine & Biologics, AiBLE, Enabling Technologies, and Advanced Energy to support surgeons and improve outcomes in complex spine and cranial procedures. Through connected technologies, navigation, robotics, imaging, and data-driven solutions, CST helps advance procedural precision, efficiency, and consistency across the continuum of care.

This is an onsite position. The individual selected for this role will work primarily from the assigned Medtronic site and collaborate closely with cross-functional engineering, quality, and product development teams. Travel is expected approximately 10-20% of the time.

As a Test Engineer II, you will support the verification and validation of software and system-level medical device products. This role contributes to the development of test strategies, automated and manual test solutions, and execution of testing activities that help ensure product performance, quality, reliability, and compliance with applicable regulatory requirements.

Primary Responsibilities
  • Develop verification and validation strategies, test plans, protocols, and reports for software and system-level products.
  • Design, implement, execute, and maintain automated and manual test solutions to support product development and release activities.
  • Create, develop, and maintain test software, tools, fixtures, and supporting test infrastructure.
  • Collaborate with cross-functional teams to review product requirements, design documentation, usability considerations, risk analyses, and defect investigations.
  • Analyze test results, document findings, and recommend corrective actions or product improvements.
  • Coordinate testing activities, including work conducted at external test facilities, and ensure test equipment remains maintained and calibrated as required.
  • Support defect tracking, troubleshooting, debugging, and root cause investigations for product and system issues.
  • Identify and implement process improvements that enhance testing efficiency, product quality, and regulatory compliance.


Required Qualifications
  • Bachelor's degree in Engineering or Computer Science and 2+ years of relevant experience, OR Master's degree, OR PhD.
  • Knowledge of applicable medical device standards and regulations, including Association for the Advancement of Medical Instrumentation (AAMI), International Organization for Standardization (ISO), U.S. Food and Drug Administration (FDA), and European Norm (EN) standards.
  • Working knowledge of software design, development, debugging, and testing practices.
  • Experience documenting and executing verification and validation activities for software and/or system-level products.
  • Effective verbal and written communication skills and the ability to work collaboratively within cross-functional teams.


Preferred Qualifications
  • Experience within the medical device industry and knowledge of FDA Quality System Regulations (QSR).
  • Experience developing automated test frameworks and executing graphical user interface (GUI), integration, and stress testing.
  • Experience with Linux, Cypress, Selenium, JavaScript, C++, Python, Perl, SQL, XML, or continuous integration tools.
  • Knowledge of Agile software development methodologies and iterative development practices.
  • Experience applying statistical methods, project planning, estimation, tracking, and technical problem solving within product development environments.


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.

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 [redacted].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 [redacted].

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):$84,800.00 - $127,200.00

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

Similar Jobs

More Jobs at Medtronic

More Pharmaceuticals & Biotech Jobs

Find similar Test Engineer II jobs: