Auditor is a seasoned Medical Device Auditor based in Japan, possessing lead auditor qualifications for ISO 13485, MDD, MDR, 9001, MDSAP, and UKMDR. With over 200 global audits conducted, including onsite, offsite, 3rd party, and unannounced audits, Auditor specializes in various regulations, spanning Australia, Brazil, Canada, Japan, and the USA. Responsibilities include audit planning, report preparation, customer interaction, and provision of training on quality management systems. With a background in electronics engineering and experience across manufacturing and service industries, Auditor offers a unique blend of technical expertise and managerial skills.