Who we are

We are here to improve lives by restoring sight worldwide by a robotic platform for vision saving surgery. Our company will improve the way ophthalmic surgery is delivered to vision impaired individuals now and for decades to come.

We are rapidly growing, funded by leading international VCs, and are looking to expand our small, motivated, multi-disciplinary and phenomenal team. Joining us is an opportunity to work towards saving vision across the globe, collaborating with others to realize a dream, and tackle an enormous challenge that will help drive your career forward.

Who we are looking for

We are looking for a Configuration Control Engineer to manage product BOMs & DMRs, oversee engineering changes (ECOs), and maintain production files. This role includes supporting design transfer and NPI activities, collaborating with engineers, manufacturers, and suppliers, and ensuring seamless data integration into ERP and PLM systems. If you're experienced in configuration management and change control processes, we’d love to hear from you!

Responsibilities

• Configuration management and Implementation of Engineering Changes/ECO.
• Manage product BOM & DMR, maintain production files (Drawings, SOP’s, Specifications, Work instructions, Test procedures, Labels, etc.)
• Lead Engineering activities and tasks in support of configuration control and Change control requirements.
• Support Design Transfer and NPI activities.
• Work with external parties – Electronic and Mechanical engineers, manufacturers, suppliers, and subcontractors.
• Responsibility for tracking information transfer to the ERP and PLM systems.
• Supporting on-going Engineering change control Workflows.

Qualifications

• Bachelor's degree in Mechanical Engineering, Industrial Engineering, or a related field.
• 5+ years’ experience in similar roles.
• Experience in transferring multidisciplinary products from development to production and managing engineering changes.
• Experience with ERP and PDM/PLM systems.
• Hands-on experience with SolidWorks.
• Knowledge of medical regulatory standards (ISO 13485, CFR 21 820) – an advantage.
• Excellent communication skills in English & Hebrew.
• Independent, hands-on, and able to manage multiple tasks efficiently.