Regulatory Affairs Specialist Toàn thời gian

Phòng 09, lầu 10, tòa nhà The Everrich 1, số 968 đường Ba Tháng Hai, Phường 15, Quận 11, Tp.Hồ Chí Minh
600$ - 1000$

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Mô Tả Công Việc

- Register many kind of dossiers, such as: new registration, renewal, quota, supplement…
- Discuss the related registration dossiers with QA,QC, R&D team...
- Receive drug dossiers from manufacturer.
- Submit supplement dossier following DAV’s request.
- Follow up and update the circular and regulation of DAV-MOH in related issues, update the related changes if any.
- Provide the registration documents of new product which had Registration No.
- Support other departments to perform comply with the regulations on the registration, advertising, studying and purchasing in Vietnam.
- Other jobs under control by Manager.

Yêu Cầu Công Việc

- Pharmaceutical/Medical University graduated.
- At least 2-year experience as R&D or Quality Control.
- Good English skills (Reading/ Speaking/ Listening/ Writing).
- Good office computer skills (Word/ PowerPoint/ Excel).
- Strong analytical, communication and time management skills.
- Ability to work collaboratively in a team.
- Familiarity with medical terminology is required.

Địa Điểm Làm Việc

968 Đường 3/2, phường 15, Quận 11
Công việc tương tự

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