Mô tả công việc
• Be responsible for all submission of registration dossiers, import quota, letters to
• Monitor the registration status of all products in DAV and other regulatory agencies.
• Follow to get approval of marketing authorization, import quota, variations in
• Compile and maintain regulatory documentation database on server.
• Establish and maintain relationships with Health Authority at staff level.
• Handle administrative works such as photocopying, notarization…
• Other tasks are assigned by Line manager.
Yêu cầu công việc
• Medicinal/Pharma certification
• Ability to work independently as well as in team.
• Possess keen interest in engaging with Health Authority and regulatory work.
• Ownership, collaboration, measured risk taking, adding value.
• Able to handle administrative duties, priority setting
• Good skill for MS Office (Word, Excel and PowerPoint).
• Knowledge of Vietnam regulation preferred.
• No English requirement.
Quyền lợi được hưởng
- 13th month salary
Thông tin liên hệ
- Người liên hệ: abbott
- Địa chỉ: