Regulatory Affairs Specialist (cs @ Tokyo)

Medtronic UK

Tokyo, Japan
Medical device regulatory affairs
Communication with overseas manufacturers
Technical english reading
Be a bridge to deliver meaningful medical devices to Japanese patients

Job Summary

  • Be a bridge to deliver meaningful medical devices to Japanese patients.
  • Develop and execute regulatory submission strategies in cooperation with overseas manufacturers and internal departments.
  • Medtronic offers a competitive Salary and flexible Benefits Package with a commitment to employee well-being.

Matching Summary

Be a bridge to deliver meaningful medical devices to Japanese patients.

Skills & Requirements

Must-have

  • Medical device regulatory affairs
  • Communication with overseas manufacturers
  • Technical English reading
  • Japanese regulatory law understanding
  • Excellent Japanese and English writing
  • Multitasking and coordination skills
  • Project management capabilities

Nice-to-have

  • Class IV medical device experience
  • Logical thinking ability
  • Learning ability for product knowledge
  • Experience with overseas counterparts

Key Requirements

  • Bachelor's degree or equivalent
  • Medical device regulatory affairs experience
  • English proficiency for communication and negotiation
  • Basic understanding of Japanese regulatory laws
  • Strong writing skills in Japanese and English
  • Multitasking and coordination skills
  • Project management skills
  • Logical thinking skills
  • Communication and negotiation skills
  • Experience working with overseas counterparts
  • General PC skills (Word, Excel, PowerPoint)
  • Ability to learn product knowledge

Work Rights

Not specified

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