Verification & Validation Specialist

Develop and maintain V&V strategy, plans, and protocols for ventilator systems in compliance with regulatory and quality standards.

 Define test methodologies for system-level, subsystem-level (hardware, software & mechanical), and component-level verification and validation.

 Lead execution of functional, safety, and performance testing across all system layers.

 Analyze test results, identify deviations, and drive resolution through root cause analysis and corrective actions.

 Provide V&V input during design transfer and manufacturing readiness reviews.

 Document test outcomes, traceability, and compliance evidence in accordance with:

o FDA 21 CFR Part 820.30 (Design Controls)

o ISO 13485 (Quality Management Systems)

o ISO 14971 (Risk Management)

o IEC 60601 / ISO 80601 (Medical Electrical & Respiratory Devices)

 Maintain audit-ready documentation including test protocols, reports, traceability matrices, and defect logs.

 Support regulatory submissions by providing V&V documentation and technical justifications.

 Collaborate with design, systems, software, mechanical, and quality teams to ensure testability and coverage.

 Participate in design reviews, risk assessments, and change control boards.

 Proficient in V&V tools, requirement management platforms like IBM DOORS, and lifecycle tools such as HP ALM.

Education & Skills preferred:

 MTech / ME / BE / BTech in Biomedical, Electrical, Mechanical, or Systems Engineering.

 3–6 years of experience in V&V for medical devices.

 Experience with ventilators, CPAP, BiPAP, or similar life-support systems is highly preferred.

 Strong understanding of design controls, risk management, and regulatory frameworks.

 Experience with test development, execution, and documentation in a regulated environment.

 Strong analytical, documentation, and commu