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Job Description
Structured overview of role & requirementsAbout This Role
Develop and execute verification and validation activities for complex electro-mechanical medical device systems ensuring complete requirements coverage.
Design, implement, and maintain automated testing frameworks and manual test protocols aligned to system and product requirements.
Collaborate cross-functionally to maintain design control documentation, identify risks, and continuously improve testing methodologies and product quality.
Minimum Requirements
Bachelor's or Master's degree in Computer Science, Electronics Engineering, or Electrical Engineering.
8+ years of software testing experience, including test protocol development and execution of verification/validation activities.
Experience with software test automation frameworks, requirements management, and design control in regulated environments.
No travel required; location based in India with a flex work model.
Ideal Candidate Profile
Background in testing software-based systems within regulated medical device or similar safety-critical industries.
Experience with automated testing tools and frameworks such as Ranorex, Playwright, Selenium, and programming with C#, .NET, or Python.
Familiarity with FDA software regulations and medical device standards (ISO 13485, ISO 14971, IEC 62304).