Quality Engineer

Microbot Medical is a cutting-edge medical device endovascular robotic surgery company, seeking an experienced, motivated Quality Engineer to join our team.We are on a mission to redefine endovascular procedures with the LIBERTY® Endovascular Robotic System, a remote, single-use and fully disposable robotic system for endovascular procedures. Across the three spaces of the endovascular market which includes peripheral, coronary and neurovascular, it is one of the largest markets with clear unmet needs, but still with minimal penetration of robotics. LIBERTY is designed to redefine the endovascular surgical robotics marketplace by overcoming many obstacles that hinder the adoption of other robotic systems by eliminating the large capital footprint and its expense, and creating a system that is easy to use, requires short learning curve, and has the potential to add value for all stakeholders.Objective:Microbot is seeking an experienced Quality Engineer. The successful candidate will join a dynamic company and will report to the VP of RA/QA.The candidate will support QA and Production activities to ensure Quality Management System compliance with ISO 13485, QMSR, MDR.Main Responsibilities:Primary Responsibilities in ProductionMonitor in-process quality controls and production line inspections, including incoming, in-process and finish goods quality controls.Monitor production-related non-conformities and corrective actionsReview production documentation (DHRs) for accuracy and complianceOversee production manufacturing activities (including production in cleanroom)Oversee acceptance, performance and routine maintenance of equipment calibration and maintenance activitiesAdditional QA SupportSupport quality records and activities follow-up, including CAPAs and MRB/NCRSupport supplier qualification and evaluationSupport training/qualification and competency activities with follow-upAssist with internal and external auditsManage document control activitiesProvide QA support to other departments/employeesEducation and ExperienceBachelor’s 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)SkillsStrong communication and teamwork abilitiesExcellent technical comprehensionProficient in English (reading and writing)Proficient in standard MS Office applications