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Kees Eilander is a seasoned professional with extensive experience in quality assurance (QA) and regulatory affairs (RA) within the medical device software industry. Currently serving as the QA/RA manager at Orikami since October 2021, Kees is responsible for the certification of the Quality Management System (QMS) for ISO 13485 and Medical Device Regulation (MDR). Prior roles include QA/RA manager Europe at Varex Imaging Corporation, where Kees managed the quality and regulatory department for medical device development and production, and Quality Manager at Philips Innovation Services, overseeing ISO 13485 quality systems. Kees' career began in quality analysis at Eurasem and spans multiple positions that emphasize expertise in quality engineering, software development for test and measurement, and project leadership across various technology sectors. Kees holds multiple relevant certifications and degrees in engineering and quality management, including a Bachelor of Science in Mechanical Engineering from Hogere Technische School Tilburg.