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Tier-1 brand, generalist Engineering Manager title, metro location, broad cross-functional requirements increase competition.
Highly specialized electro-mechanical and medical-device regulatory expertise limits cross-industry transferability.
Explicit 15+ years requirement plus 10+ years electro-mechanical experience and medical-device regulatory mandates make shortlisting very strict.
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Manage a cross-functional engineering team (firmware, mechanical, hardware, systems) developing electro-mechanical medical devices focused on motor drives, electric hardware, and controller firmware.
Oversee technical design reviews, ensure compliance to medical device standards and regulations (IEC 60601, IEC 62304, ISO 13485, ISO 14971) and guide product development and verification processes.
Lead global cross-functional stakeholder management, talent development, and technical innovation for medical device product and technology roadmap delivery.
Bachelor's degree in Electronics & Communication Engineering or Electrical Engineering; Master's degree preferred.
Minimum 15 years product development experience with at least 10 years in electro-mechanical device development and verification.
Strong hands-on experience in motor controllers, firmware development, mechanical design of drive trains, hardware development, and systems integration.
Knowledge of medical device regulatory standards (IEC 60601, IEC 62304, ISO 13485, ISO 14971) and design controls for medical device development.
Highly experienced leader capable of managing global, cross-functional electro-mechanical engineering teams in medical device development.
Demonstrated ability to oversee complex product design, verification, and compliance activities in regulated healthcare environments.
Proven track record of delivering innovative motor controller and electro-mechanical solutions aligning with medical device technology roadmaps and business goals.