Back
Strong Tier-1 brand but regulated-device specialization reduces applicant density.
Regulated medical-device QA and IEC62304 familiarity makes cross-industry moves difficult.
Multiple explicit filters including 8+ years, test-framework architecture, and regulated medical device experience.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Lead design and execution of test plans and strategies for medical device software applications, ensuring compliance with standards like IEC62304.
Develop and maintain automated and manual tests using tools such as Appium, Selenium, and BDD frameworks; support test infrastructure including simulators and emulators.
Provide hands-on leadership, mentoring, and software engineering best practices to junior engineers while collaborating across cross-functional teams globally.
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 programming languages such as Java, JavaScript, Groovy, Python, or Objective C.
Experience with automated/manual testing tools (Appium, Selenium), BDD tools (SpecFlow, Cucumber, Gherkin), and familiarity with Agile and Waterfall methodologies.
Experienced in developing and verifying software within regulated medical device environments with understanding of IEC62304.
Capable of independently translating high-level requirements into test designs and able to lead technical discussions across global teams.
Strong background in implementing test automation frameworks and test infrastructure, able to mentor junior staff and drive quality improvements.