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

MSD (Merck)

Tokyo, Japan
Hybrid
Experience in pharmaceutical development
Regulatory submission coordination
Knowledge of pharmaceutical regulations
Develop an efficient and high value-added Japan regulatory development strategy in line with global strategies

Job Summary

  • Develop an efficient and high value-added Japan regulatory development strategy in line with global strategies.
  • Responsible as a contact person with regulatory authorities such as MHLW and PMDA.
  • Contribute to improving the quality of documents submitted to authorities through thorough review and advice.

Matching Summary

Develop an efficient and high value-added Japan regulatory development strategy in line with global strategies.

Skills & Requirements

Must-have

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

Nice-to-have

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

Key Requirements

  • Experience working at a pharmaceutical company
  • Master of Life Sciences or above
  • English communication skills

Work Rights

Not specified

Tailored Resume

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