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Participant in development of multidisciplinary project end to end Full Stack
The development shall be mostly in C # and C ++
Lead development tasks through all stages gathering requirements, planning, performing DRs and full implementation.
Design and implement various features on a wide range of platforms.
Work closely with system and HW engineers, SW developers, QA and many more.
Perform design and code reviews and system integrations.
Constant collaboration and knowledge sharing with the SW team.

you will be an integral part of the design control process, working alongside a collaborative, multi-disciplinary team of software, electrical, mechanical, control, and systems engineers. You will be responsible for planning, executing, and documenting V V activities for complex electro-medical systems, ensuring compliance, performance, and safety across all phases of development. This is a hands-on role requiring technical depth, systems-level perspective, and cross-functional coordination.

We are seeking a highly skilled Real-Time C ++ and Python software engineer to join our dynamic team. The ideal candidate will have extensive experience in developing and optimizing software for Real-Time systems, ensuring high performance and reliability. This role involves working on cutting-edge projects that require a deep understanding of the theoretical and practical aspects of Real-Time computing, with proficiency in both C ++ and Python.

Responsibilities:
Design, develop, and maintain software for Real-Time systems using C ++ and Python.
Optimize software to meet performance requirements and ensure low latency and high reliability.
Collaborate with cross-functional teams to define software requirements and specifications.
Implement and TEST software modules to ensure they meet the necessary performance and safety standards.

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!