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Location
In office (Caesarea)
Seniority
Junior · 2+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Nov 2, 2026. First seen by Alion on Nov 2, 2026. Medtronic scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Medtronic is one of the largest medical device manufacturers in the world, founded in a Minneapolis garage in 1949 as a repair shop for hospital equipment before building the first wearable cardiac pacemaker. Its portfolio now spans cardiac rhythm devices, heart valves, neuromodulation and neurosurgery, surgical stapling and robotics, spinal implants and diabetes management systems sold in more than one hundred and fifty countries. The company is legally domiciled in Ireland after its 2015 combination with Covidien, while its operational headquarters and most of its research remain in Minnesota.
Backed by NEA, Menlo Ventures, 8VC

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

Join a multidisciplinary Research & Development (R&D) team focused on developing and sustaining innovative surgical platforms that support improved patient outcomes. This team is responsible for verification and validation of complex medical systems that integrate software, hardware, and algorithms while ensuring compliance with quality and regulatory standards.

As a Software Test Engineer, you will support the verification and validation of complex multidisciplinary medical systems. Working closely with Software, Systems Engineering, Quality, Regulatory, and Verification & Validation teams, you will execute system-level testing activities, investigate product issues, validate software performance, and contribute to maintaining high standards of product quality and compliance.

Primary Responsibilities:

  • Design, develop, and execute system-level software verification tests
  • Create and perform test cases validating software interactions within multidisciplinary medical systems
  • Verify end-to-end workflows, interfaces, data flow, and system behavior against product requirements
  • Analyze test results, identify trends and product risks, and document findings
  • Investigate defects, support root-cause analysis, validate fixes, and perform regression testing
  • Author test protocols, traceability documentation, and formal verification reports in compliance with quality and regulatory requirements
  • Develop and maintain test automation tools and scripts to improve testing efficiency and coverage
  • Support released-product activities including sustaining projects, corrective and preventive actions (CAPAs), software updates, and product enhancements

Required Qualifications:

  • Bachelor's degree in Software Engineering, Computer Engineering, Electrical Engineering, Mechanical Engineering, Biomedical Engineering, or related engineering discipline AND 2+ years of experience in software testing, verification and validation, algorithm validation, or system integration
  • Experience testing multidisciplinary systems that incorporate software, hardware, and algorithms
  • Experience developing and executing verification test plans, test cases, and test documentation
  • Knowledge of software defect investigation, root-cause analysis, and regression testing
  • Availability to work on-site in Caesarea at least 3 days per week

Preferred Qualifications:

  • Experience in the medical device or other regulated industry
  • Experience with test automation tools, scripting, or automation framework development
  • Programming skills and understanding of system integration concepts
  • Experience working with cross-functional engineering teams in product development or sustaining environments
  • Knowledge of quality system and regulatory requirements applicable to medical devices

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.

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 @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 [email protected].

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.

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
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