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