Summary:

Results-driven Software & Systems Verification Engineer with 5+ years of experience in FDA-regulated medical devices, embedded systems, and molecular diagnostics. Expertise in Software Verification & Validation (V&V), automated testing, embedded firmware validation, and risk-based testing aligned with IEC 62304, ISO 13485, ISO 14971, IEC 62366, IEC 60601/61010, and FDA 21 CFR Part 11/820 regulations. Proven success in validating infusion pumps, hemodialysis systems, and PCR-based diagnostic platforms while supporting FDA 510(k) submissions, CAPA, and audit readiness.

Key Responsibilities:

• Develop, execute, and maintain software/system verification protocols and test strategies for FDA-regulated medical devices.


• Perform functional, integration, regression, and system-level testing for embedded software and firmware applications.


• Validate safety-critical workflows inclu...