GE HealthCare Healthcare/BioTech

Verification and Validation Lead

India In person Full-time

Location: IND19-01-Bengaluru-EPIP 122 (Phase II)

Job Description Summary

We are seeking an experienced Verification & Validation Lead to drive quality, compliance, and product verification for software-intensive medical devices and connected healthcare solutions.

This role will lead end-to-end verification and validation activities across the product lifecycle, ensuring products meet regulatory, safety, performance, and quality requirements. The ideal candidate combines strong V&V leadership with hands-on expertise in test automation, system verification, and regulated product development.

GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.

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Key Responsibilities

  • Lead verification and validation activities for software, systems, and integrated medical device solutions.
  • Define verification strategies, test plans, protocols, and quality metrics aligned with product requirements, risk management, and regulatory expectations.
  • Ensure complete traceability between requirements, risk controls, verification evidence, defects, and release deliverables.
  • Drive risk-based verification approaches in compliance with ISO 14971 and medical device quality processes.
  • Develop and maintain automated test frameworks for system, integration, API, regression, and end-to-end testing.
  • Enhance test infrastructure, simulation environments, and CI/CD pipelines to improve automation, coverage, and efficiency.
  • Lead defect triage, root cause analysis, and resolution planning for product quality issues.
  • Contribute to verification of system performance, reliability, scalability, interoperability, and other critical product characteristics.
  • Collaborate with Software, Systems, Quality, Regulatory, Clinical, and Product teams throughout the development lifecycle.
  • Mentor verification engineers and promote best practices in quality engineering, automation, and regulatory compliance.
  • Support design reviews, risk assessments, audits, CAPA activities, and regulatory submissions.

Job description provided by GE HealthCare.
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