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Metro location and known multinational brand create moderate competition despite senior, specialized QA requirement.
Requires regulated medical device verification and standards expertise, so background fit is highly industry-specific.
Explicit 10+ years and regulated medical device verification experience make shortlisting highly strict.
Lead verification team to design and implement verification environments, tests, and coverage metrics ensuring design specifications and quality standards are met.
Coordinate debugging and drive delivery of verified design blocks meeting functionality, performance, and coverage requirements.
Oversee development and documentation of test cases, risk identification and mitigation, and coordinate verification activities throughout SDLC within Agile teams.
Bachelor’s or Master’s degree in Computer Science, Computer Engineering, Electrical Engineering, Software Engineering or related field.
10+ years of related experience in regulated software development (preferably medical devices or similarly regulated domains).
Experience leading small to medium technical teams and working in Agile/Scrum environments.
Strong knowledge of verification strategies including functional, non-functional, reliability, performance testing; experience with test automation frameworks and test architecture.
Experienced in regulated software development, especially medical device software or other highly regulated products like aviation software.
Skilled in defining test strategies, test architecture, and test automation with proven track record of delivering quality in Agile setups.
Capable of global collaboration, risk management, and improving test execution quality and delivery with tools like ALM and JIRA; knowledge of IEC 62304, ISO 14971 standards preferred.