R&D ENGINEER

In this role, you will take a medical device from initial concept to production — designing the electronics, mechanics, and firmware, and preparing the regulatory documentation behind them. This is hands-on engineering with real hardware, in a small team where one engineer owns the entire project. For over 30 years, Medoc has been a leader in the medical device industry, developing, manufacturing, and marketing advanced devices that diagnose how the sensory nervous system functions. Our products are considered the industry standard — FDA-approved and CE-certified — and are used worldwide in neurology, pain research, and related fields. What you%27ll do • Take a development project end to end: from defining requirements through design, verification, and transition to production. • Work with stakeholders across the company to translate product requirements into clear technical and engineering specifications. • Take ownership of the engineering design across the full stack: electronics, mechanics, embedded software and UI, algorithms, thermal analysis, and signal processing. • Plan and run design verification and validation %28V&V%29 testing — build the tests, review the results, and stand behind the conclusion that requirements are met. • Document each stage of the project and lead design reviews. • Take ownership of your project%27s regulatory documentation — you are responsible not just for producing it, but for making sure it is accurate — and support other regulatory tasks as needed. • Lead the transfer to production, from planning through execution. What we%27re looking for • BSc in Biomedical, Mechanical, or Electrical Engineering. • 2+ years of experience developing multidisciplinary products that combine hardware, mechanics, and software in the same box. We%27re flexible on seniority — the scope will match your experience. • Strong, hands-on expertise in at least two of the following: finite element and thermal analysis, PCB design %28KiCad or similar%29, CAD %28SolidWorks or similar%29, embedded development, or signal processing in MATLAB/Python. Breadth across the rest matters more than a checklist. • Quick to learn unfamiliar tools and codebases, including AI-assisted development and analysis — paired with the discipline to verify your own work before it becomes part of the official design. • Strong engineering judgment — able to identify, analyze, and solve complex problems, and to tell the difference between an answer that sounds right and one that actually is right. • Comfortable navigating literature and patents and judging what%27s actually credible. • Excellent verbal and written communication in Hebrew and English — a must%21 • Self-driven, versatile, and effective both independently and alongside colleagues across departments. Nice to have • Background in the medical or healthcare field — clinical, research, or industry is an advantage. • Experience with medical device quality systems %28ISO 13485, FDA design controls%29. • Prior work taking a regulated product through verification and into production.