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Medium due to strong employer brand and metro location, but senior niche V&V specialization reduces applicant density.
High because deep medical-device V&V, regulatory, and compliance expertise is domain-specific and less transferable.
High because explicit multi-tier experience, regulatory V&V expertise, and managerial requirements are mandatory.
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Own and advance Software Quality & V&V organization at Medtronic Engineering India Center (MEIC).
Direct software test strategy, automation frameworks, defect management, and regulatory compliance across multiple product lines.
Manage V&V project execution, align resources with strategic milestones, and liaise with global R&D teams for superior product safety and performance.
Bachelor's degree in Computer Science, Electronics/Electrical, Biomedical Engineering, or equivalent.
18+ years total experience in software engineering, test engineering, and product quality in a global product development environment.
8+ years hands-on experience in Software Verification & Validation (V&V) including test automation architectures.
5+ years software engineering management experience overseeing V&V/QA initiatives with proven large team leadership.
Experienced leader with a strong record in medical device software quality standards and regulated industry compliance (IEC 62304, FDA 21 CFR, ISO 13485, ISO 14971).
Proven ability driving test efficiency via automation, CI/CD integration, and managing defect lifecycles in complex software.
Skilled at managing global cross-functional partnerships including R&D, Regulatory, Quality Assurance, with strong decision-making on release readiness and quality gates.