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Salary
≈ $12k – $29k per year (Estimated)
Location
In office (Hyderabad)
Seniority
Senior · 8+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 22, 2026. First seen by Alion on Oct 1, 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

The Mazor Robotics Program within Medtronic develops software-enabled technologies that support complex medical device systems used in patient care. This role is part of the Verification and Validation (V&V) function, focused on ensuring product quality through test strategy development, requirements traceability, manual testing, and test automation across complex electro-mechanical systems.

This position is based in India and follows a Flex work model, combining remote and in-office work. No travel is required for this role.

This role is responsible for developing and executing verification and validation activities for complex medical device systems. The Senior Enterprise Software Engineer partners with cross-functional engineering teams to translate product requirements into test protocols, establish automated testing solutions, maintain design control documentation, and ensure complete requirements coverage throughout the product development lifecycle.

Primary Responsibilities

  • Develop test protocols and validation strategies based on system and product requirements.
  • Design, implement, and maintain automated test frameworks and test scenarios.
  • Execute system-level and software-level verification activities for complex electro-mechanical products.
  • Perform requirements traceability analysis to ensure complete test coverage.
  • Create and maintain design control documentation in accordance with Quality Management System requirements.
  • Collaborate with software, systems, hardware, and quality engineering teams to resolve product issues and testing challenges.
  • Identify technical risks, limitations, and verification gaps and recommend mitigation strategies.
  • Support continuous improvement of test methodologies, automation approaches, and product quality practices.

Required Qualifications

  • Bachelor's degree OR Master's degree in Computer Science, Electronics Engineering, or Electrical Engineering with 8+ years of software testing experience.
  • Experience developing test protocols and executing verification and validation activities for software-based systems.
  • Experience with software test automation frameworks and automated testing methodologies.
  • Experience with requirements management tools and configuration management tools.
  • Experience documenting and maintaining design control artifacts within regulated development environments.

Preferred Qualifications

  • Experience testing medical devices or other regulated products.
  • Experience with Ranorex, Playwright, Selenium, C#, .NET, and Python.
  • Knowledge of Food and Drug Administration (FDA) software regulations and guidance.
  • Knowledge of ISO 13485, ISO 14971, IEC 62304, and related medical device standards.
  • Experience working with cross-functional engineering teams in product development environments.

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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