Associate Principal Regulatory Specialist

Dyson

Tokyo, Japan
Japan quasi-drug regulatory compliance
Japanese cosmetic regulations
Pmd act, pmda processes
This role serves as the Japan regulatory subject matter expert within the Global Regulatory team, ensuring compliance with the PMD Act and supporting product development for global market access

Job Summary

  • This role serves as the Japan regulatory subject matter expert within the Global Regulatory team, ensuring compliance with the PMD Act and supporting product development for global market access.
  • Key responsibilities include managing Japan quasi-drug and cosmetic regulatory compliance, product classification, labeling, ingredient compliance, and post-market obligations.
  • The position requires independent management of global regulatory projects, clear communication of compliance requirements, and participation in team transformation initiatives.

Matching Summary

This role serves as the Japan regulatory subject matter expert within the Global Regulatory team, ensuring compliance with the PMD Act and supporting product development for global market access.

Skills & Requirements

Must-have

  • Japan quasi-drug regulatory compliance
  • Japanese cosmetic regulations
  • PMD Act, PMDA processes
  • GQP/GVP requirements
  • QMS knowledge
  • regulatory submissions and notifications

Nice-to-have

  • think differently and challenge convention
  • collaborative and enthusiastic team
  • passionate about what we do
  • flexibly work on multiple categories

Key Requirements

  • 8+ years Japan regulatory affairs experience
  • Expertise in quasi-drugs and cosmetics
  • Ability to carry legal accountability
  • Fluent Japanese and strong English communication
  • Pharmacist license preferred

Work Rights

Not specified

Tailored Resume

Cover Letter