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Strong employer brand, Bangalore metro role, and mid-level experience range increase applicant competition.
Medical device integration and regulated-process requirements make cross-industry transitions difficult.
Explicit 6–11 years, ISTQB, FDA/ISO knowledge and test tool mandates increase screening strictness.
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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, and provide actionable feedback to development and core teams for issue resolution and product quality improvements.
Support test estimation and planning, including realistic scheduling, scope definition, and risk assessments, while driving continuous improvement in test methodologies and tools.
B.E / M.C.A or equivalent degree in Computer Science, Electronics, or a related discipline.
6 to 11 years of experience in test engineering, preferably in system integration and verification.
ISTQB Foundation Level certification is mandatory.
Office-based role located in Bangalore, India; onsite presence required at least 3 days per week.
Strong technical understanding across hardware and software development lifecycles with emphasis on integration and verification.
Experience working within process-oriented, regulated environments (FDA and/or ISO) and hands-on familiarity with test management tools like HP ALM, Clear Quest, or TFS.
Able to manage dynamic and changing priorities in a complex R&D setting, focusing on quality and accuracy with a process-driven approach.