Project Manager Medical Device Development Mumbai (India)

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: Bachelors/Masters in Engineering (Mechanical, Electrical, Electronics, Biomedical, or Software). 1015 years of experience in medical device development or regulated technical projects. Hands-on understanding of hardware, firmware, and Mechanical development lifecycle. Robust 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. Translate technical requirements into project plans and execution strategies. Track progress, manage dependencies, and ensure on-time delivery Cross-Functional Technical Coordination Act as the bridge between design teams: hardware, firmware, mechanical, and systems. Facilitate technical discussions, design trade-offs, and architecture decisions Technical Risk & Issue Management Identify, assess, and mitigate technical risks across hardware, firmware, and mechanical. Maintain risk registers and technical issue logs. Ensure timely resolution of technical blockers Vendor & Supplier Technical Management Coordinate with contract manufacturers, suppliers, and design partners. Ensure technical deliverables meet quality, compliance, and performance standards Tools & Technologies Project Management: MS Project, Jira Documentation Risk management tools Collaboration platforms (Confluence, Teams, Share Point) 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: Bachelors/Masters in Engineering (Mechanical, Electrical, Electronics, Biomedical, or Software). 1015 years of experience in medical device development or regulated technical projects. Hands-on understanding of hardware, firmware, and Mechanical development lifecycle. Robust 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. Translate technical requirements into project plans and execution strategies. Track progress, manage dependencies, and ensure on-time delivery Cross-Functional Technical Coordination Act as the bridge between design teams: hardware, firmware, mechanical, and systems. Facilitate technical discussions, design trade-offs, and architecture decisions Technical Risk & Issue Management Identify, assess, and mitigate technical risks across hardware, firmware, and mechanical. Maintain risk registers and technical issue logs. Ensure timely resolution of technical blockers Vendor & Supplier Technical Management Coordinate with contract manufacturers, suppliers, and design partners. Ensure technical deliverables meet quality, compliance, and performance standards Tools & Technologies Project Management: MS Project, Jira Documentation Risk management tools Collaboration platforms (Confluence, Teams, Share Point)