לוח משרות דרושים ייצור ותעשייה

We are a leading company in the fields of functional neurosurgery and neuroscience research. With over two decades of industry experience, we are committed to improving neurology and neurosurgery patient care by developing superior technology solutions. Our mission is to provide tools for those working to reveal the mysteries of the brain and find cures for neurological disorders. We strive for the highest standards of reliability, quality, and customer support, while fostering employee development and serving our community.
Role Description:
This is a full-time on-site role for a Quality Control Specialist at Tsipporit. The Quality Control Specialist will be responsible building our products according to DMR. performing final tests. PCBA & Cable functional inspection. Modules Visual & functional inspection.
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ART MEDICAL is a well-funded, medical startup developing cutting-edge technologies for ICU patients. Our smART+™ platform is an intelligent, sensor-based feeding system for critical care patients that aims to prevent life-threatening in-hospital complications, such as ventilator-associated pneumonia, malnutrition, and acute kidney injury. With the introduction of Nutrition Management 2.0™ to critical care patient scoring systems, the smART+™ platform monitors, analyzes, and prevents malnutrition and gastric aspiration in real-time. By providing optimal nutritional care and achieving up to 100% feeding efficiency, the smART+™ platform improves the standard of care and helps ICU patients recover faster. As a System Engineer, reporting to The System Engineering Manager, You will be part of a multidisciplinary group of system, hardware, firmware, software and software test engineers. You will serve as an internal and external technical liaison for multiple interfaces in the organization and externally you will drive medical products into the next level of maturity and performance to meet the user and business needs. Main position duties:
* Translate user needs into actionable technical system requirements
* Manage system, sub-system and software requirements of Medical devices
* Responsibility for development of the system architecture and top-level design
* Work in a multidisciplinary and complex technical environment
* Perform risks management activities for product and production
* Act as the technical lead of multidisciplinary medical system and subsystems
* Responsibility for the system functionality, performance and quality
* Translate field and production feedback into product and production improvements
* Work closely with multidisciplinary R&D team V&V, regulatory, quality and more
* Write V&V test plans and test methods
* Participate and lead product life cycle processes
* Perform R&D projects planning and tasks breakdown