Đăng ký thuốc (RA)

Responsibilities:

Support company in commercial supply by providing technical documents to Marketing team as and when necessary
Follow up DAV expert and VFA expert to get registration approval within deadline given by company
Perform other tasks required by Line Manager
Review of products Dossiers for Drug formulation, Food supplements and submit to DAV, VFA as per requirement
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
Regulatory submission for Imported as well as some of the Local products

Requirement:
Work Experience

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

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Cập nhật gần nhất lúc: 2024-06-16 10:45:02