Lead regulatory strategy and execution for veterinary pharmaceuticals, vaccines, and biologicals in Japan, ensuring compliance with MAFF (Ministry of Agriculture, Forestry and Fisheries) and PMDA requirements.

Manage end-to-end product registration, renewals, and post-approval changes, maintaining alignment with Japanese regulatory standards and timelines.

Serve as the primary contact with Japanese regulatory bodies, driving transparent communication and resolution of regulatory queries or audits.

Collaborate closely with local and global R&D, QA, and commercial teams to support product development and go-to-market strategies in Japan.

Monitor evolving Japanese regulatory policies and guidelines, providing expert insight to leadership on risk mitigation and business implications.

Please send your CV to admin@managray.com