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Tier-1 brand, metro location, and broad generalist QA requirements make competition high.
Core QA skills transfer across industries, but medical device regulatory knowledge raises domain specificity.
Explicit 8+ years, premium-institute degree requirement, and regulated-medical device experience increase strictness.
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Lead test engineering decisions and design automated and manual tests for software validation, including in regulated medical device environments.
Develop, execute, and maintain test plans and frameworks in collaboration with development and systems engineering teams globally.
Provide technical leadership, mentorship, and support to junior engineers while contributing to test infrastructure and tool development.
Bachelor's degree in Computer Science, Bio-Technology, Bio-Medical, Electronics, or Electrical Engineering from a premium institute.
8+ years of software industry experience including 5+ years in software/test framework design and architecture.
Proficiency in one or more languages: Java, JavaScript, Groovy, Python, Objective C or equivalent.
Experience with automated testing tools and frameworks like Appium, Selenium, SpecFlow, Cucumber, or Gherkin; familiarity with medical device software standards (IEC62304) preferred.
Experienced in both manual and automated testing within regulated, medical device software development environments.
Comfortable working in agile and waterfall development processes and collaborating across global, cross-functional teams.
Demonstrates ability to lead testing strategy, mentor engineers, and improve test tools and processes to enhance team productivity.