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Tier-1 employer and Bangalore metro increase applicant density despite niche medical-device specialization.
Regulated medical-device integration verification requires domain-specific experience, limiting cross-industry transferability.
Explicit 6–11 years, ISTQB, FDA/ISO knowledge, and specific tools make shortlisting highly strict.
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Design, prepare, and execute integration, subsystem, and system-level verification tests for MR products based on defined requirements.
Analyze, document, and report test results; collaborate with development teams on defect investigation, root cause analysis, and validation of fixes.
Support test estimation and planning; contribute to schedule, scope, and risk assessments; implement improvements in test practices and tools.
Bachelor's degree (B.E) / Master's in Computer Applications (M.C.A) or equivalent in Computer Science, Electronics, or related discipline.
6 to 11 years of experience in test engineering, preferably in system integration and verification environments.
ISTQB Foundation Level certification required.
Experience with test management tools such as HP ALM, ClearQuest, or TFS.
Strong technical understanding of hardware and software development lifecycles, including integration and verification phases.
Process-oriented mindset with familiarity of FDA and/or ISO regulated environments.
Ability to work in a complex R&D setting with dynamic priorities, focusing on quality, accuracy, and collaboration across cross-functional teams.