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Tier-1 brand, metro location, generalist senior QA title, and broad skillset increase competition.
Automation skills are transferable, but regulated medical-device experience increases domain specificity to medium.
Explicit 8+ years, 5+ framework years, and regulated-medical requirements make shortlisting highly strict.
Lead test engineering decisions and design test plans and strategies for software projects in a regulated medical device environment.
Develop, execute, and maintain automated and manual tests ensuring traceability from requirements to verification.
Provide technical leadership and mentorship to junior engineers and collaborate with global cross-functional teams to support debugging and quality assurance.
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 at least 5 years in software/test framework design and architecture.
Proficiency with programming languages such as Java, JavaScript, Python, Groovy, Objective C or equivalents; experience with BDD test tools (SpecFlow, Cucumber, Gherkin) is advantageous.
Experience with automated test tools (Appium, Selenium) and familiarity with Android and iOS operating systems; experience in regulated medical device software testing preferred.
Experienced in software testing and test framework architecture for regulated medical devices aligning with standards like IEC62304.
Able to independently lead test strategy and execution while mentoring junior engineers in a fast-paced, multi-disciplinary environment.
Strong collaborator with exposure to Agile and Waterfall methodologies, comfortable working with globally distributed teams and cross-functional stakeholders.