R&d Regulatory Affairs Sr. Scientist（開発薬事）

Merck & Co., Inc.

Hybrid
Pharmaceutical company experience
Drug approval application experience
Life sciences master's degree
The role involves building efficient and high value-added domestic drug development strategies aligned with global goals

Job Summary

  • The role involves building efficient and high value-added domestic drug development strategies aligned with global goals.
  • Candidates will serve as the primary contact person for regulatory authorities such as the MHLW and PMDA.
  • Responsibilities include coordinating the preparation and submission of NDA documents and managing internal schedules with US headquarters.

Matching Summary

The role involves building efficient and high value-added domestic drug development strategies aligned with global goals.

Skills & Requirements

Must-have

  • Pharmaceutical company experience
  • Drug approval application experience
  • Life sciences master's degree
  • English literature reading skills
  • Regulatory authority communication

Nice-to-have

  • Positive attitude
  • Logical thinking skills
  • Initiative and action-oriented
  • Knowledge of Pharmaceutical Affairs Regulations

Key Requirements

  • Master of Life Sciences or above
  • Experience in filing and review processes
  • Work experience at a pharmaceutical company

Work Rights

Not specified

Tailored Resume

Cover Letter