Medical Device Tester- Systems Verification Engineer

About the Role

• 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. ). • 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