QUỐC TẾ SƠN HÀ

Mô tả Công việc
Responsibilities:
Review of products Dossiers for Drug formulation, Food supplements and submit to DAV, VFA as per requirement
Regulatory submission for Imported as well as some of the Local products
Technical support for Technology transfer projects for Group companies
Review and submission of technical documents for Tender application
Candidate will be responsible for GMP registration required for Tender application
Follow up DAV expert and VFA expert to get registration approval within deadline given by company
Support company in commercial supply by providing technical documents to Marketing team as and when necessary
Perform other tasks required by Line Manager
Review of products Dossiers for Drug formulation, Food supplements and submit to DAV, VFA as per requirement
Regulatory submission for Imported as well as some of the Local products
Technical support for Technology transfer projects for Group companies
Review and submission of technical documents for Tender application
Candidate will be responsible for GMP registration required for Tender application
Follow up DAV expert and VFA expert to get registration approval within deadline given by company
Support company in commercial supply by providing technical documents to Marketing team as and when necessary
Perform other tasks required by Line ManagerYêu Cầu Công Việc
Requirement:
Work Experience
Graduated from medical university.
Responsibility to work, hard work, good self-learning ability, initiative and positive thinking.
2-3 years of experience in drug registration.
Good organizational and time management skills.Laptop
Chế độ bảo hiểm
Du Lịch
Phụ cấp
Du lịch nước ngoài
Chế độ thưởng
Chăm sóc sức khỏe
Đào tạo
Tăng lương
Công tác phí
Phụ cấp thâm niên
Nghỉ phép năm
CLB thể thao