[innovative Medicine] R&d, Director, Japan Medical Writing, Regulatory Medical Writing, Global Development

Johnson & Johnson MedTech

Chiyoda, Japan
Regulatory medical writing expertise
Strategic and operational leadership
Cross-functional team collaboration
The Director of Regulatory Medical Writing is accountable for the strategic and operational leadership of Reg MW activities for Japan and China

Job Summary

  • The Director of Regulatory Medical Writing is accountable for the strategic and operational leadership of Reg MW activities for Japan and China.
  • This role requires strong partnership and close collaboration with senior functional and matrix leaders across Innovative Medicine R&D (IMRD) organization in Japan and China.
  • Responsible for creating an environment where employees feel engaged and empowered, and take pride in their role, responsibilities, and deliverables.

Matching Summary

The Director of Regulatory Medical Writing is accountable for the strategic and operational leadership of Reg MW activities for Japan and China.

Skills & Requirements

Must-have

  • Regulatory Medical Writing expertise
  • strategic and operational leadership
  • cross-functional team collaboration
  • process improvements and best practices
  • document planning and content
  • resource management and allocation

Nice-to-have

  • inclusive work environment
  • motivate and develop talent
  • positive Credo-based work environment
  • openness to new ideas

Key Requirements

  • University/college degree in scientific discipline
  • 14 years relevant pharmaceutical/scientific experience
  • 12 years relevant clinical/medical writing experience
  • 5 years people management experience
  • Expertise in project management
  • Expertise in process improvement

Work Rights

Not specified

Tailored Resume

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