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 overseas regulatory specialist supports Konica Minolta’s diagnostic devices, medical IT and AI-enabled healthcare products. The role anticipates changes in international medical-device regulations and standards and combines technical understanding with regulatory strategy to support compliant market access.
Responsibilities include monitoring overseas requirements, obtaining product authorizations and developing approval strategies with planning, development, production, sales and service teams. The specialist decides whether new products or changes to existing specifications need applications, and collaborates with regulatory colleagues in Japan and overseas. Complex imaging products and emerging AI/security rules form part of the operating context.
Applicants need at least five years of medical-device regulation, standards and quality-management experience, plus understanding of overseas device rules such as FDA, MDR, China or ASEAN frameworks.
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