Your responsibilities 

• Lead the architecture, design, and development of software for medical devices


• Coordinate and mentor a team of software engineers


• Collaborate with hardware, QA, regulatory and industrial design teams


• Oversee the full development lifecycle: requirements, architecture, implementation, integration, and validation


• Ensure compliance with applicable regulatory standards (IEC , ISO , etc.)


• Participate in code reviews, risk analyses, and architecture evaluations


• Manage technical project planning: estimates, priorities, risks, milestones, and deliverables


• Ensure software quality through the implementation of testing and automation practices


• Interact directly with clients to define requirements and technical solutions

Your profile

• 8+ years of professional software development ...