Medicaroid is a Japan based medical device company founded 2013 with its global Headquarter in Kobe. As the Head Regulatory affairs and of Quality Management, you will be an integral part of supervising the regulatory and quality matters at Medicaroid hinotoriTM robotic surgery system. You will be responsible for managing the team and drive results in accordance with MDR (Medical Device Regulation 2017/745) and ISO 13485 requirements. You will collaborate with other departments, such as Medical, Commercial, Customer Support & Service, Logistics, Alliance & Engineering, Training/Education and Marketing. * Lead the preparation and maintenance of plans and annual reports in accordance with MDR (Medical Device Regulation 2017/745) and ISO 13485 requirements * Take accountability, lead and manage the quality and regulatory affairs team, ensuring drive, high quality output, ...
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