Associate Manager, Regulatory Affairs

Stryker

Tokyo, Japan
Hybrid
6+ years of medical device experience
Approval applications for medical devices
Qms compliance inspection applications
The role involves executing approval applications and notifications for medical devices manufactured by Stryker Japan K.K

Job Summary

  • The role involves executing approval applications and notifications for medical devices manufactured by Stryker Japan K.K.
  • Candidates must have a strong understanding of relevant laws and regulations.
  • Effective communication with internal departments is essential for success in this position.

Matching Summary

The role involves executing approval applications and notifications for medical devices manufactured by Stryker Japan K.K.

Skills & Requirements

Must-have

  • 6+ years of medical device experience
  • Approval applications for medical devices
  • QMS compliance inspection applications

Nice-to-have

  • Good communication skills
  • Project management skills
  • Integrity and action-oriented mindset

Key Requirements

  • Experience with PMDA consultation
  • Ability to write business documents
  • Experience with Class I to IV application approvals

Work Rights

Not specified

Tailored Resume

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