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Tier-1 brand, metro location, and mid-level generalist QA title increase applicant competition.
Medical-device integration QA requires regulated, hardware-software expertise, limiting cross-industry transferability.
Explicit 3+ years, ISTQB certification, regulated-environment and tool requirements increase filter rigidity.
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Design, prepare, and execute integration, subsystem, and system-level verification tests for MR products covering functional and non-functional aspects.
Analyze, document, and report test results; manage defect tracking and collaborate with development teams for root cause analysis and fix validation.
Support test estimation, planning, and continuous improvement of test engineering practices and tools within a regulated R&D environment.
Bachelor's degree (B.E/M.C.A) in Computer Science, Electronics, or related discipline.
3+ years of experience in test engineering, preferably in system integration and verification environments.
ISTQB Foundation Level certification and hands-on experience with test management tools like HP ALM, Clear Quest, or TFS.
Office-based role requiring presence in Bangalore; experience or knowledge of FDA and/or ISO regulated environments is expected.
Experienced in both hardware and software development lifecycles, specifically integration and verification phases.
Process-oriented with focus on quality, accuracy, and ability to manage changing priorities in a complex R&D setting.
Strong collaborator capable of working across global, cross-functional R&D teams in regulated environments.