【r&d】薬事申請グループ スタッフ / Post Approval Change Management

Pfizer

Tokyo, Japan
Regulatory change management
Teamwork and communication skills
Basic it skills
The role is responsible for regulatory activities related to post-approval CMC change management for pharmaceutical products

Job Summary

  • The role is responsible for regulatory activities related to post-approval CMC change management for pharmaceutical products.
  • The candidate will manage product approval changes to maintain a stable product supply.
  • The position involves developing regulatory strategies and internal processes through cross-functional collaboration.

Matching Summary

The role is responsible for regulatory activities related to post-approval CMC change management for pharmaceutical products.

Skills & Requirements

Must-have

  • Regulatory change management
  • Teamwork and communication skills
  • Basic IT skills

Nice-to-have

  • Experience with PMDA interaction
  • Knowledge of drug characteristics
  • Industry association involvement

Key Requirements

  • Graduated science college/university
  • Knowledge of local regulatory law
  • English speaking and writing skills

Work Rights

Not specified

Tailored Resume

Cover Letter