概要

• 給与

  4,000 SGD ~ 4,500 SGD

• 業界

  Manufacturing(Pharmaceutical/Medical Equipment)

• 仕事内容

  Our client, a Japanese pharmaceutical company, is currently seeking to hire a Regulatory Affairs Specialist (Japanese speaking) to support operations across Asia and the ASEAN region. The primary responsibilities of this role include coordinating regulatory submissions, supporting strategy development, and monitoring activities across local affiliates.
  
  You will be reporting to the Regulatory Affairs Department in Japan.
  
  【 Responsibilities 】
  ‐ Handle mainly regulatory operations tasks
  - Report directly to the Regulatory Affairs Department in Japan
  - Coordinate regulatory submissions (new and variation) across Asia/ASEAN
  - Manage regulatory documents and ensure timely submissions
  - Develop regulatory strategies with cross-functional teams
  - Track and monitor local affiliate regulatory activities
  - Identify and resolve regulatory issues proactively