Manage group cash, funding and credit and foreign-exchange risks, support global treasury operations and work with domestic and overseas finance teams.
About this role
This regulatory-affairs specialist supports Konica Minolta’s healthcare products, including diagnostic imaging and medical IT. The role focuses on Japan’s medical-device rules while collaborating with regulatory colleagues internationally, helping the business respond to changing standards and increasingly complex products incorporating AI image processing.
Responsibilities include monitoring domestic regulations and standards, obtaining product authorizations, and designing approval strategies aligned with business plans. The specialist works with planning, development, production, sales and service teams and determines whether new products or changes to existing specifications require authorization applications.
Applicants need at least five years of experience relating to medical-device regulations, standards and quality management, and understanding of device regulation under Japan’s pharmaceutical and medical-device law.
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