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We're looking for a hands-on Embedded engineer to join our growing core robotics team. If you're passionate about high-performance Real-Time systems, motor control, or industrial protocols like EtherCAT, this is your opportunity to work on a truly cutting-edge humanoid robot.
Youll design, implement, and optimize Embedded code for Real-Time control of actuators, sensors, and communication layers running directly on STM32 microcontrollers all bare metal, no OS. This is not application-level development its close to the metal, critical-path firmware engineering.
Responsibilities
Design and develop Real-Time firmware in C for STM32-based robotic subsystems.
Write precise, efficient, and maintainable code for motor control, IO handling, safety loops, and communication.
Work with high-speed buses, ADCs, DMA, interrupts, timers, and peripherals.

We seek a team lead with a strong technical background and proven leadership
experience to join our growing company. The ideal candidate will guide a team of skilled developers, ensuring the delivery of high-quality SaaS platforms and hybrid solutions. This role requires a balance of hands-on technical expertise and strong interpersonal skills to foster collaboration and alignment with the product team.

As part of our commitment to excellence and growth, we are seeking a Senior Developer with extensive experience in Web and Mobile development. This role is not just about coding, it's about growing. You will be a member of a dynamic engineering team and help shape our product architecture

Company: Cortex-Dental 
Location: Shlomi (North)
 
Department: QA/RA
Reports To: VP QA/RA

Job Description:
We are seeking an experienced Regulatory Affairs Specialist to join our team and contribute to the development, implementation, and management of regulatory processes within the company.
The ideal candidate will be responsible for communication with external regulatory bodies such as Notified body, EUDAMED, authorized representative. In addition will be responsible for analyzing and understanding regulatory requirements, providing guidance to various departments, executing regulatory registrations in multiple regions such as Asia, Europe north and south America  and ensuring compliance with applicable regulations.

Key Responsibilities:
- Analyze and interpret new regulations in the medical device industry.
- Provide advice and guidance to internal teams on regulatory requirements.
- Develop and implement policies and procedures to meet regulatory standards.
- Conduct risk assessments.
- Represent the company in interactions with regulatory agencies and governmental bodies.
- Prepare reports and reviews on compliance status.
- Performing regulatory registration processes

If you are interested in joining a leading team in the regulatory affairs sector, please send your resume with the subject line "Regulatory Affairs Specialist Application."
We look forward to hearing from you!