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Requirements:
For a cutting-edge medical device company, we are seeking an experienced, motivated software engineer to join our team. Main Responsibilities:
*The candidate will be responsible for the software development of a medical robot in a fastgrowing environment and will be charged with developing Embedded code and support testing and HW activities.
*Design, develop, and maintain Embedded software for robotic medical systems
*Develop, maintain and management of SW for production and testing of assembly line instruments
*Develop and maintain drivers and interfaces
*Implement and TEST communication protocols
*Support HW, Mechanics, and V&V activities
*Participate in code reviews and maintain software quality standards and ensure compliance with medical device regulations and software development standards
*Optimize, and improve existing software systems
*Collaborate in cross-functional teams (R&D and Operations), contributing to both design and implementation decisions
*Contribute to project planning, timelines, and deliverables for Embedded software development Requirements:
*B.Sc. in SW Engineering/ Computer Science / Electrical engineering / Practical Electrical Engineer with relevant background
*Over 5 years of experience as an Embedded software engineer with the following qualifications:
o Knowledge in software languages:
C proficient
Python must
C ++, JAVA, Kotlin, C #, Dart nice to have
o Must have experience with low level and drivers programming
o Experience in SPI, UART, I2C, TCP, UDP, etc. nice to have
o Knowledge of RF communication protocols (WiFi, BLE, SUBG) nice to have
o Knowledge in IAR or equivalent tools.
*Experience in the medical devices industry a significant advantage
*Ability to understand and implement electronic components specification and schemes
* data base development and management an advantage
*Must be a team-player but capable of handling a project end to end.

Requirements:
For a cutting-edge medical device company, we are seeking an experienced, motivated Quality Engineer to join our team. Main Responsibilities:
*Primary Responsibilities in Production
*Monitor in-process quality controls and production line inspections, including incoming, in-process and finish goods quality controls.
*Monitor production-related non-conformities and corrective actions
*Review production documentation (DHRs) for accuracy and compliance
*Oversee production manufacturing activities (including production in cleanroom)
*Oversee acceptance, performance and routine maintenance of equipment calibration and maintenance activities Additional QA Support
*Support quality records and activities follow-up, including CAPAs and MRB/NCR
*Support supplier qualification and evaluation
*Support training/qualification and competency activities with follow-up
*Assist with internal and external audits
*Manage document control activities
*Provide QA support to other departments/employees Education and Experience:
*Bachelors degree in science or engineering (Mechanical, Biomedical, or related)
*Minimum 3 years' experience as quality engineer/ QC activities in medical device industry (ISO 13485, FDA QMSR, MDR) Skills
*Strong communication and teamwork abilities
*Excellent technical comprehension
*Proficient in English (reading and writing)
*Proficient in standard MS Office applications Skills:
*Strong communication and teamwork abilities
*Excellent technical comprehension