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Metro location and established global brand increase applicants, but medical-device QA niche and seniority limit competition.
Regulated medical-device verification expertise and IEC 62304 knowledge strongly limit cross-industry transferability.
Mandatory 10+ years plus regulated medical-device verification and test-automation experience tighten candidate filters.
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Lead the verification team in designing and executing verification environments, test-benches, stimulus, and coverage metrics for software/hardware designs.
Coordinate debugging of test failures with design teams and ensure verified design blocks meet functionality, performance, and coverage criteria for sign-off.
Drive development and documentation of product test cases, manage testing risks with mitigation plans, and oversee verification activities during SDLC under Agile methodologies.
Bachelor's or Master's degree in Computer Science, Computer Engineering, Electrical Engineering, Software Engineering, or related field.
10+ years of related experience in software testing/verification.
Demonstrated experience in regulated software development, preferably medical devices or similarly regulated domains.
Experience working in Agile/Scrum development process.
Experienced technical leader capable of managing small to medium technical teams and improving team performance.
Strong background in defining test strategies, architectures, and automation frameworks, particularly for regulated software products.
Familiar with medical device software standards (e.g., IEC 62304, ISO 14971) and skilled in tools like ALM, JIRA; automation experience (e.g., Selenium) is preferred.