Japan - Tokyo
permanent
Industry RegulationCross-functional CollaborationEnglish CommunicationBasic IT SkillsPharmacovigilance knowledgeCMC ManagementPMDA Interaction Experience
1. Job Objective: Responsible for regulatory activities related to post‑approval CMC (Chemistry, Manufacturing and Controls) change management for pharmaceutical products, contributing to the mainten...
March 10, 2026
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