【COMPANY OVERVIEW】
An American Orthopedics Medical Device company.
【JOB RESPONSIBILITIES】
Responsible to fulfill the duties for foreign manufacturers under Japanese law.
Get approval, maintain, and renew QMS conformity and foreign manufacturer's registration.
【WHY YOU SHOULD APPLY】
Promising career path.
Work with industry leaders and global businesses.
Work with the latest technology in orthopedics industry.
【REQUIREMENTS】
At least 3 years of Foreign Manufacturer Registration (FMR) experience in Medical Device and/or Pharmaceutical industry and QMS conformity survey application OR medical device registration.
Fluent in Japanese.
Authorized to work in Japan.