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

Merck Sharp & Dohme Corp

Hybrid
Experience in pharmaceutical development
Regulatory submission coordination
Knowledge of pharmaceutical regulations
The role involves developing a high value-added regulatory strategy for new drug development in Japan

Job Summary

  • The role involves developing a high value-added regulatory strategy for new drug development in Japan.
  • You will be the main contact with regulatory authorities and contribute to improving the quality of submitted documents.
  • Coordination with headquarters and relevant parties is essential during the regulatory submission process.

Matching Summary

The role involves developing a high value-added regulatory strategy for new drug development in Japan.

Skills & Requirements

Must-have

  • Experience in pharmaceutical development
  • Regulatory submission coordination
  • Knowledge of pharmaceutical regulations

Nice-to-have

  • Strong communication skills
  • Positive and logical thinking
  • Initiative and action-oriented

Key Requirements

  • Experience with approval submissions
  • Master's degree in Life Sciences or above
  • Basic knowledge of pharmacy or medicine

Work Rights

Not specified

Tailored Resume

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