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. This role will involve all topics which are related to the regulatory and quality environment including the support for joint development of devices as quality and regulatory expert. * Oversee the QMS to ensure compliance with quality standards * Take accountability, lead and manage the quality and regulatory affairs team, ensuring drive, high quality output, wellbeing and development of the * Minimum of 7 years' experience in managing a multi-disciplinary regulatory and quality team, or regulatory and quality teams cumulative experience * Deep knowledge of QMS, product safety laws, operational quality, and global market regulatory requirements
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