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Popular mid-level QA role in Bangalore with a 5-7 year band increases candidate competition.
Medical device V&V and IEC 62304 expertise is highly domain-specific and not easily transferable across industries.
Mandatory 5+ years and regulated medical device V&V experience narrows candidate pool significantly.
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Own and execute test strategy, including design and documentation of test cases, workflows, and data management for medical device software.
Lead and collaborate with verification teams to improve test execution, quality, and delivery ensuring adherence to standards such as IEC 62304 and ISO 14971.
Plan and execute system integration and verification activities, ensuring traceability from requirements to verification and design entities.
5+ years of full-time work experience in software testing or verification for regulated software development.
Bachelor's or Master's degree in Computer Science, Computer Engineering, Electrical Engineering, Software Engineering, or related field.
Location requirement: Bangalore – PSN, Whitefield; full-time, 5 days a week.
Mandatory skills include manual and device testing for medical device software and knowledge of verification strategies (functional, non-functional, reliability, performance).
Experienced in regulated software development environments, preferably medical devices or similarly regulated sectors (e.g., aviation software).
Proven technical leadership in medium to large Verification & Validation (VnV) teams with ability to lead small to medium-sized teams technically.
Familiar with Agile/Scrum processes and enterprise software automation tools with knowledge of test architecture and automation framework design.