Tuyển Regulatory Affairs Executive
Mô tả công việc
• Check and review all required documents of the application for import license for categories of company products (Medicines, biologicals, vaccines, cosmetics, food supplement, medical devices, clinical trial material,…).
• Prepare import application for special controlled drugs, medical devices.
• Submit import application to competent organs.
• Closely follow up the status of application from the time of submission until getting approval.
• Assist the preparation reports relating to special controlled drugs sent to competent organs as
stipulated.
• Daily update and inform Regulatory Import Manager the status of application submission, MOH and feedback on application until the completion of work.
• Update and send report of assigned tasks to Department Head.
• Assist the other company Dept. in following up the submitted applications with MOH/DAV such as price declaration or other assigned tasks.
Yêu cầu công việc
• University graduation.
• Have 2 - 3 years working experience at a similar role.
• Business acumen and deep understanding in pharma market.
• Hardworking, accurate and well-organized.
• Ability of maintaining and developing the relationship with MOH, DOH.
• Good communication in English - Vietnamese.
• Proficiency in Microsoft Offices (Word, Excel, Powerpoint).
Phúc lợi công việc
• Deal with the company.
Cách thức ứng tuyển
Ứng viên nộp hồ sơ trực tuyến bằng cách bấm nút Nộp đơn dưới đây
Công ty TNHH Zuellig Pharma Việt Nam
24/10/2020
Tp Hồ Chí Minh
Nhân viên/ Có kinh nghiệm
Pháp chế doanh nghiệp
Tiếng Anh
Đại học
2 năm
Nam nữ
Công ty TNHH Zuellig Pharma Việt Nam