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Senior, niche V&V role in regulated medical devices reduces applicant pool despite Thermo Fisher's strong brand.
Domain-specific regulated medical-device V&V skills limit cross-industry transferability.
Explicit 12+ years plus regulated V&V and technical mandatory skills create stringent hiring filters.
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Own verification and validation of software and system functionality for Clinical and Industrial Analyzer platforms, including desktop and instrument software, hardware-software integration, and cybersecurity.
Design, develop, and execute comprehensive verification plans and automated test frameworks, ensuring traceability to system and software requirements.
Collaborate with cross-functional teams to validate new features, resolve defects, support regulatory compliance, and improve product quality throughout lifecycle.
Bachelor's or Master's degree in Software Engineering, Computer Science, Electronics, Information Technology, Systems Engineering, or related discipline.
Minimum 12 years of experience in Software Verification & Validation, Software Quality Engineering, Systems Verification, or Product Validation.
Experience testing desktop applications and instrument-based software systems in regulated environments (preferred: Medical Devices, Clinical Diagnostics, Life Sciences, Industrial Instrumentation).
Proficiency with automation frameworks (e.g., Selenium, NUnit), Windows and Linux software validation, communication protocols (TCP/IP, USB), and cybersecurity testing.
Experienced in Agile development environments (Scrum, Kanban, SAFe) with strong systems engineering knowledge and ability to handle complex multidisciplinary product verification.
Practiced in designing and executing verification strategies that include hardware-software interaction, regulatory compliance, and traceability management.
Skilled at collaborating across global cross-functional teams, analyzing defects, debugging, and enhancing V&V automation and processes.