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

med-in.at

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

Job Summary

  • The role involves developing efficient and high value-added domestic regulatory 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 interactions with US headquarters.

Matching Summary

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

Skills & Requirements

Must-have

  • Pharmaceutical company experience
  • Drug approval application experience
  • Life sciences master degree required
  • English literature reading capability
  • Cross-border communication skills

Nice-to-have

  • Positive thinking attitude
  • Logical reasoning abilities
  • Proactive initiative style
  • Knowledge of Pharmaceutical Affairs Regulations

Key Requirements

  • Master's degree in Life Sciences
  • Experience in filing and review processes
  • Background in pharmaceutical development

Work Rights

Not specified

Tailored Resume

Cover Letter