System Software Engineer

We are seeking a dedicated System Engineer with a strong software background who thrives in multidisciplinary environments involving complex hardware and software systems. This role is ideal for a motivated individual eager to contribute to a groundbreaking ophthalmic robotic platform. You'll play a key role in shaping the next generation of ophthalmic surgical technologies.

Who we are:

At ForSight Robotics, we are united behind our mission: we believe that robotic ophthalmic surgery is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a pioneer and market leader in ophthalmic robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. We lead with inclusion and empower our team members to do their best work as their most authentic selves.

• Our office is currently located in Yoqneam Illit and will be relocating to Caesarea, near the train station, in October 2025.
  
  

• Translate user, product, and marketing requirements into detailed software system and subsystem specifications.
• Manage software-related system requirements and operational parameters.
• Partition complex software systems into manageable subsystems, modules, and components.
• Lead software integration within multidisciplinary engineering teams.
• Oversee software verification and validation activities at subsystem and system levels.
• Collaborate closely with regulatory teams for software compliance with medical device standards and regulations.
• Coordinate with project managers to create and maintain accurate software project schedules.
  
  

• Bachelor's degree in Electrical Engineering or Computer Engineering or Aeronautics from a recognized university (Master's degree preferred).
• Minimum 5 years of experience as a System Engineer in multidisciplinary environments.
• Hands-on experience in software engineering.
• Experience working in a medical device company - advantage.
• Familiarity with medical device compliance and relevant standards (ISO 60601, 62304, 14971, 13485) - advantage.
• Experience in Verification & Validation (V&V) processes - advantage.
• Strong experience with hardware interfaces.
• Excellent documentation skills and fluency in technical English (verbal & written).
• Ability to self-manage projects and lead technical discussions.