Regulatory Affairs Specialist

Location 東京都
Discipline Life Science
Job type Permanent
Salary NEGOTIABLE
Reference 34410

COMPANY OVERVIEW

A US based company focused oncology diagnosis

 

JOB RESPONSIBILITIES

  • Responsible for maintaining regulatory approvals for medical devices in Japan

  • Consultation with PMDA and creating strategies in line with their feedback

  • Review labelling

  • Development and review of SOPs

  • Analyse regulatory challenges before they arise and provide solutions

 

REQUIREMENTS

  • Minimum of 2 years of experience in regulatory affairs. (IVD/Medical Device preferred)

  • Japanese and English abilities

 

FOR FURTHER INFORMATION

  • Click apply

OR

  • Contact Pauline

pauline.mares@cornerstone.jp