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Senior, regulated-medical-device QA at Medtronic narrows applicant pool despite strong brand.
Regulated medical-device standards and embedded/mobile testing demands make cross-industry transferability limited.
Explicit 8+ years plus mandatory testing frameworks, automation tools, and regulated-device experience tighten filters.
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Own the design and execution of software test plans and strategies, including both automated and manual testing for medical device software.
Lead test engineering decisions, collaborate with developers and systems engineers to align on application specifics and platform requirements.
Provide hands-on leadership and mentorship to junior engineers, develop reusable testing tools and patterns, and maintain test infrastructure including tools and simulators.
Bachelor's degree in Computer Science, Bio-Technology, Bio-Medical, Electronics, or Electrical Engineering from a premium institute.
8+ years of software industry experience with 5+ years in software/test framework design and architecture.
Proficiency in programming languages such as Java, JavaScript, Groovy, Python, or Objective C.
Experience with automated testing tools (e.g., Appium, Selenium) and knowledge of medical device software standards (IEC62304) preferred but not strictly mandatory.
Experienced working in regulated medical device software environments and familiar with software verification processes in such contexts.
Demonstrates ability to lead cross-functional teams involving software development, verification, system engineering, and quality assurance.
Strong in both manual and automated test development with experience in test frameworks (BDD tools like SpecFlow, Cucumber, or Gherkin is a plus) and software lifecycle methodologies (Agile and Waterfall).