Regulatory Affairs Specialist (cs @ Tokyo)

Medtronic UK

Tokyo, Japan
Competitive salary; short-term incentive (mip) ava...
Medical device regulatory approval experience
Japanese and english communication skills
Understanding of pmd act regulations
The primary mission is to act as a bridge delivering meaningful medical devices to Japanese patients

Job Summary

  • The primary mission is to act as a bridge delivering meaningful medical devices to Japanese patients.
  • Responsibilities include developing regulatory approval strategies, creating high-quality applications, and coordinating with domestic and international departments.
  • Medtronic offers a competitive salary, flexible benefits package, and eligibility for the Medtronic Incentive Plan.

Matching Summary

The primary mission is to act as a bridge delivering meaningful medical devices to Japanese patients.

Salary

Competitive Salary; Short-term incentive (MIP) available; Flexible Benefits Package

Skills & Requirements

Must-have

  • Medical device regulatory approval experience
  • Japanese and English communication skills
  • Understanding of PMD Act regulations
  • Project management and multitasking abilities
  • Technical document creation capabilities

Nice-to-have

  • Class IV medical device application experience
  • Experience with overseas manufacturers
  • Strong logical thinking skills
  • Ability to learn product knowledge quickly

Key Requirements

  • Bachelor's degree or equivalent qualification
  • Fluency in Japanese and English
  • Experience with Class IV medical device applications preferred

Work Rights

Not specified

Tailored Resume

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