Senior Regulatory Affairs

Location Tokyo
Discipline Life Science
Job type Permanent
Salary Up to 12,000,000 JPY
Reference 35520

COMPANY OVERVIEW

A cutting edge Medical Device company specializing in Orthopedics.

 

JOB RESPONSIBILITIES

  • Be in charge of regulatory affairs submission.

  • Apply, acquire, and sustain Japanese government approval.

  • Attend lectures and seminars related to regulations.

  • Respond to PMDA notices.

  • Formulate documents for reimbursement.

 

WHY YOU SHOULD APPLY

  • Be a part of a global medical device company.

  • Work with industry leaders and global businesses.

  • Generous earning potential.

REQUIREMENTS

  • 1-3 year experience in Medical Device Regulatory Affairs; document submissions.

  • Must have at least conversational English and fluent Japanese language ability.

  • Authorized to work in Japan.