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

AbbVie

Tokyo, Japan
Onsite
Science background required
Native japanese language proficiency
English reading and writing skills
AbbVie is seeking a Regulatory Affairs Specialist focused on medical devices, particularly in the cardiovascular field, based in Tokyo, Japan. This entry-level position is open to candidates with a scientific background and offers the opportunity to learn and grow in regulatory affairs, with a strong emphasis on collaboration and communication

Job Summary

  • The role involves creating and managing application documents for regulatory authorities to support product lifecycle management under the guidance of senior staff.
  • This position offers a unique opportunity to gain expertise in regulatory affairs for Class IV high-risk cardiovascular medical devices from an entry-level standpoint.
  • The work environment emphasizes close communication with team members and departments, providing a structured path for professional growth through daily information sharing.

Matching Summary

Match Score: 75

AbbVie is seeking a Regulatory Affairs Specialist focused on medical devices, particularly in the cardiovascular field, based in Tokyo, Japan. This entry-level position is open to candidates with a scientific background and offers the opportunity to learn and grow in regulatory affairs, with a strong emphasis on collaboration and communication.

Skills & Requirements

Must-have

  • Science background required
  • Native Japanese language proficiency
  • English reading and writing skills
  • Logical verbal communication ability
  • High accuracy in documentation
  • Willingness for morning conference calls

Nice-to-have

  • Master's degree or higher
  • Strong interest in healthcare industry
  • Experience in regulatory or quality assurance
  • Proactive learning mindset
  • Interest in cardiovascular medical devices

Key Requirements

  • Science background required
  • Native Japanese level
  • Master's degree preferred
  • Prior experience in regulatory or QA fields

Work Rights

Not specified

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