Regulatory Affairs Specialist（医療機器・循環器領域）／未経験可

Abbott

Tokyo, Japan
Science background required
Native japanese proficiency
English reading and writing skills
This role involves creating and managing regulatory submission documents for medical devices under the guidance of senior staff

Job Summary

  • This role involves creating and managing regulatory submission documents for medical devices under the guidance of senior staff.
  • The position offers a supportive environment for individuals with no prior experience to learn Regulatory Affairs expertise from the ground up.
  • Candidates will have opportunities to participate in new product approvals and lifecycle management for Class IV high-risk cardiovascular devices.

Matching Summary

This role involves creating and managing regulatory submission documents for medical devices under the guidance of senior staff.

Skills & Requirements

Must-have

  • Science background required
  • Native Japanese proficiency
  • English reading and writing skills
  • Logical verbal communication
  • Attention to detail and compliance
  • Willingness for morning international calls

Nice-to-have

  • Master's degree preferred
  • Strong interest in medical devices
  • Experience in regulatory or quality assurance
  • Growth mindset and proactive learning
  • Interest in cardiovascular field

Key Requirements

  • Science background (Bachelor's or higher)
  • Native-level Japanese language ability
  • English reading/writing capability
  • Master's degree (preferred)

Work Rights

Not specified

Tailored Resume

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