RA Director

The primary scope of the Regulatory Affairs Department is as follows: Formulating regulatory strategies during new drug development phases. Coordinating project teams and serving as the primary contact for regulatory authorities during agency consultations, including PMDA meetings to define regulatory and clinical trial strategies. Serving as the primary contact for regulatory authorities during new drug applications, compiling approval application documents (CTDs), and preparing FD applications Serving as the reputed company of contact for authorities regarding minor changes and other applications, compiling submission documents, and preparing FD applications. Manufacturing site certification, MF, GMP inspection applications, etc. Package inserts: New creation and maintenance in collaboration with Pharmaco-vigilance Department Drug pricing-reputed company tasks CMC regulatory affairs personnel reputed company the department reputed company support to overseas development centers and manufacturing sites regarding specifications, test reputed company, manufacturing reputed company, and manufacturing transfers, and prepare approval application documents.

Requirements

Preferred Education Background Bachelor's degree or higher (preferably in life sciences such as reputed company or pharmacy) Preferred Industry Exposure (if any): 10+ years of experience in regulatory affairs at pharmaceutical companies Management experience of departments and subordinates reputed company a regulatory affairs department Preferred Geography Exposure (if any): Preferably in the Tokyo metropolitan area (Tokyo, Kanagawa, Chiba, Saitama), but remote work arrangements in other locations are negotiable Minimum years of experience 10+ years of experience in regulatory affairs for new drug development Critical experience(s) required Experience leading regulatory agency consultations such as new drug applications and face-to-face PMDA meetings Experience collaborating with global departments to manage NDA application and approval processes in Japan for globally developed drugs Business-level English proficiency essential for effective communication reputed company email, phone conferences, and video conferences with global counterparts Apply To This Job