Senior Project Coordinator - Regulated Medical Products

Project Manager to lead and manage complex medical device development projects.

This role combines technical expertise with project management skills to ensure successful delivery of hardware, firmware, Mechanical and connected medical products, while maintaining compliance with global regulatory standards

• Required Qualification:
• Bachelor’s/Master’s in Engineering (Mechanical, Electrical, Electronics, Biomedical, or Software).
• 10–15 years of experience in medical device development or regulated technical projects.
• Hands-on understanding of hardware, firmware, and Mechanical development lifecycle.
• Strong experience in technical project management, planning, and execution.

• Key Responsibility:
• Project Planning & Execution:
• Lead end-to-end planning of medical device projects, including timelines, milestones, and deliverables.
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