Medical Device Tester- Systems Verification Engineer

• Bachelor’s / Master’s degree in Computer Science, Electrical Engineering, or related field (or equivalent experience).
• 8+ years of experience in System Verification & Validation (Product testing), systems engineering, with significant exposure to medical devices or regulated environments.
• Deep knowledge of medical products/systems, performance testing, and troubleshooting.
• Strong experience with mobile application testing (Android/iOS) and system integration & system testing.
• Proficiency in requirements analysis, configuration management, and issue tracking systems (Jira, Git, etc.).
• Excellent analytical, problem-solving, and communication skills.
• Proven ability to collaborate with teams across different regions.
• Test automation using Appium, Python, Selenium, API Automation and related tools (Optional).
• Good knowledge of AI tools.
• Excellent analytical skills coupled with a high level of initiative and responsibility
• Analyze and understand High Level & Low Level Design documents, Intended Use documents, Software Requirements.
• Analyze software requirements to provide timely and meaningful review feedback for testability, completeness, and consistency
• Design high level test scenarios or test considerations.
• Design system verification test cases at Integration & System level. End to End workflow & Functional tests to uncover bugs.
• Ensure requirement-test traceability and coverage.
• Estimate, Prioritize, Plan and Co-ordinate testing activities including test planning, test execution, test reporting & monitoring.
• Identify, record, Report and document defects/bugs in bug tracking tool.
• Work closely with SW team on bug fixing and improving overall product quality.
• Perform risk-based tests & Impact based tests to ensure optimal regression suites for product releases.
• Provide triage assistance when required to support faster analysis of bugs
• Coordinate with required stakeholders and teams to resolve any dependencies or impediments for testing.
• Ensure all verification and validation activities comply with ISO 13485 (Medical Devices) and ISO 14971 (Risk Management) standards.
• Eagerness to take on responsibility and natural curiosity to creatively search for software defects
• Ability to effectively execute in a complex, high-pressure environment
• Ability to conform to shifting priorities, demands and timelines
• Proven ability to work in a dynamic, multi-disciplinary team environment
• Proven relationship building skills
• Team player with excellent interpersonal and verbal