לוח אפשרויות קריירה - הדרך החכמה להייטק

In this role, you will support the implementation and maintenance of our Quality Management System (QMS), ensuring compliance with regulatory standards such as ISO 13485 and 21 CFR Part 820. You will work closely with cross-functional teams to help maintain quality processes, conduct inspections and contribute to continuous improvement initiatives.
This is an excellent opportunity to gain hands-on experience in a fast-paced, innovative startup environment while working on medical devices that make a real difference in patients' lives.