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Tier-1 brand, metro Hyderabad, and a generalist senior engineering title increase competitive density.
Strong medical-device regulatory and implantable systems experience required, limiting cross-industry transferability.
Explicit 8–12 years, 5+ years medical-device experience and regulatory requirements make filters strict.
Lead system integration and testing activities for complex medical device systems targeting central nervous system treatments.
Drive resolution of system issues and improve product designs based on customer feedback and verification outcomes.
Coordinate cross-functional teams to achieve project and quality objectives, ensuring alignment of technical deliverables and risk mitigation.
Bachelor’s degree in Engineering (M.Tech/PhD preferred).
8-12 years total professional experience.
Minimum 5 years experience in medical device industry; knowledge of ISO and Quality System Regulation mandatory.
Experience with system integration, verification & validation in regulated environments involving wireless and embedded medical device technologies.
Experienced in system engineering and integration in implantable or complex medical/electronic device systems.
Skilled in applying system engineering methodologies, translating user needs into formal requirements, and leading cross-functional teams.
Proficient in technical problem-solving including firmware/hardware troubleshooting and automated test systems in regulated environments.