Regulatory Affairs Manager/Expert - 製薬 会社

Location: Tokyo, Japan
Job Type: Permanent
Salary ¥10000000.00 - ¥11000000.00 per annum
Specialization: Life Science (Medical Devices / Pharmaceutical / Chemical / Healthcare / Agriculture / Livestock)
Sub Specialization: Regulatory Affairs
Contact: Yuichi Matsuda
Reference: JO-1909-426154
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[Company Description]
Global Pharmaceutical Company

Regulatory Affairs Manager/Expert

  • Represent Development RA group in the responsible Project Team
  • Develop submission plan in collaboration with RPM and manage/coordinate preparation of all regulatory documentation, i.e. briefing document for PMDA consultation, CTN documents, JNDA documents (CTD), etc.
  • Develop regulatory strategy for each project
  • Create HA interaction plan
  • Represent the Company in any interactions with HAs
  • Review and provide regulatory input to all regulatory documentation
  • Collect and analyze updated regulatory-related information and share with the relevant people


  • 5 or more years of experience of regulatory affairs in pharmaceutical industry
  • Proven expertise in development and management of regulatory strategy for Japan
  • Demonstrated experience in interaction with HAs in Japan
  • Experience of regulatory affairs in in vitro diagnostics/companion diagnostics development (preferable)
  • Business level English

[Desired Characteristics]

  • Proven leadership and management skills in the functional and cross-functional team
  • Good interpersonal communication skill
  • Negotiation skill
  • Business-orienting thinking

[Employment Type]
Full time

(Experiences and skills will be considered)


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