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

Merck & Co., Inc.

Hybrid
Pharmaceutical company experience
Drug approval filing experience
Life sciences master degree
The role involves developing efficient and high value-added Japan regulatory development strategies aligned with global goals

Job Summary

  • The role involves developing efficient and high value-added Japan regulatory development strategies aligned with global goals.
  • Candidates will serve as the primary contact person for regulatory authorities such as MHLW and PMDA while coordinating submission documents.
  • The position requires a Master's degree in Life Sciences along with proven experience in pharmaceutical development and drug filing processes.

Matching Summary

The role involves developing efficient and high value-added Japan regulatory development strategies aligned with global goals.

Skills & Requirements

Must-have

  • Pharmaceutical company experience
  • Drug approval filing experience
  • Life sciences master degree
  • English literature reading skills
  • Regulatory document review

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 at pharmaceutical company
  • Filing/Review experiences
  • Basic knowledge about pharmacy or medicine

Work Rights

Not specified

Tailored Resume

Cover Letter