Lead C++ Software Engineer

Lead C++ Software Engineer

Surgical Robotics : Medical Device

US Remote based Opportunity

Qt, OpenGL, VTK, OpenCV, DCMTK, and ITK

Full Time Direct Hire Position

Position Overview

Our client is developing a next-generation surgical navigation platform designed to enhance implant accuracy in orthopedic procedures. Our goal: deliver precise, intuitive guidance technology that integrates seamlessly into the surgical workflow and empowers surgeons without adding complexity.

As the Lead Software Engineer, you will own the full software development lifecycle for this advanced navigation system. You will guide architectural decisions, lead and mentor the software team, and ensure all development activities meet the rigorous standards required for safety-critical medical devices. This is a high-impact technical leadership role at the center of a system that blends real-time visualization, computer vision, robotics, and medical imaging.

Key Responsibilities

• Lead the design, development, and optimization of medical-grade software for FDA-regulated devices—particularly systems involving surgical navigation, image-guided surgery, or robotics.
• Ensure full compliance with ISO 13485, IEC 62304, and ISO 14971 throughout the software lifecycle, maintaining complete DHF, risk management, and software documentation to support regulatory submissions.
• Architect, implement, and refine software solutions in C++, focusing on real-time performance, reliability, and safety.
• Integrate and apply advanced frameworks Qt, OpenGL, VTK, OpenCV, DCMTK, and ITK to enable high-performance visualization, imaging workflows, and data processing.
• Develop algorithms and systems for robotics, computer vision, image processing, homography, kinematics modeling, and embedded device communication.
• Manage software project planning using modern tools (e.g., JIRA), ensuring alignment with the product roadmap, including milestones, deliverables, and cross-functional dependencies.
• Drive CI/CD pipeline development, ensuring automated, reliable, and traceable software verification.
• Communicate effectively with clinical, product, and engineering stakeholders; translate complex technical considerations into clear, actionable insights.
• Work in a fast-moving startup environment—balancing leadership, hands-on development, and autonomous execution.
• Uphold rigorous data security and cybersecurity standards, particularly regarding sensitive patient data and medical imaging workflows.

Qualifications

• BS + 8 years, MS + 6 years, or PhD + 4 years in Computer Science, Computer Engineering, or related discipline.
• 3+ years of software leadership experience, ideally within regulated medical device development.
• Demonstrated experience developing software under FDA regulations, with deep familiarity with ISO 13485 and IEC 62304.
• Hands-on experience with ISO 14971 risk management.
• Expertise in C++, object-oriented programming, and modern software architecture.
• Experience with Qt, VTK, OpenCV, ITK, and related visualization or imaging frameworks.
• Background in one or more of the following: robotics, computer vision, image processing, homography, software architecture, or kinematics.
• Strong record of delivering complex, safety-critical software solutions in dynamic environments.
• Excellent communication skills and ability to perform well both independently and in collaborative teams.
• Experience with CI/CD pipeline implementation and software project management tools.

Preferred Qualifications

• Experience integrating with PACS systems, managing DICOM images, and ensuring secure access during clinical workflows.
• Familiarity with cybersecurity and data protection requirements for medical devices.