Đăng Ký Thuốc (Ra)

Responsibilities:

Technical support for Technology transfer projects for Group companies
Support company in commercial supply by providing technical documents to Marketing team as and when necessary
Regulatory submission for Imported as well as some of the Local products
Candidate will be responsible for GMP registration required for Tender application
Review of products Dossiers for Drug formulation, Food supplements and submit to DAV, VFA as per requirement
Perform other tasks required by Line Manager
Review and submission of technical documents for Tender application
Follow up DAV expert and VFA expert to get registration approval within deadline given by company

Requirement:
Work Experience

2- 3 years of experience in drug registration.
Good organizational and time management skills.
Graduated from medical university.
Responsibility to work, hard work, good self- learning ability, initiative and positive thinking.

- Tăng lương
- Phụ cấp thâm niên
- Phụ cấp
- Du Lịch
- Chế độ bảo hiểm
- Chăm sóc sức khỏe
- Công tác phí
- Du lịch nước ngoài
- Laptop
- Chế độ thưởng
- CLB thể thao
- Nghỉ phép năm
- Đào tạo

Cập nhật gần nhất lúc: 2024-07-18 01:50:03