Check with seller Tuyển dụng Hà Nội Công ty TNHH Zuellig Pharma Việt Nam cần tuyển

[Tuyển dụng Hà Nội] Công ty TNHH Zuellig Pharma Việt Nam cần tuyển Chi tiết công việc

Giới thiệu công ty



Thu nhập:
Cạnh tranh
Loại hình:
Toàn thời gian





Chức vụ:
Nhân viên





Kinh nghiệm:
5 năm
dược phẩm
pháp lý
y tế
Mô tả công việc
Mô tả Công việc
POSITION: REGULATORY AFFAIRS EXECUTIVE (TEMP 6 MONTH)
- Work location: Lot B3, Cong Nghiep 4 Str, Sai Dong B Industrila Park, Long Bien, Hanoi
- Report to: Head of Regulatory Affairs
MAIN DUTIES:
· Evaluate and review registration dossiers for administration
· Prepare registration dosier, ensure that the drug registration dossiers submitted to the authorities on time with accurate information
· Closely follow up the status of application from the time of submission until getting approval.
· Communicate clearly with the DAV staff/experts and AbbVie RA on the query if any, based on the scientific of drug registration and regulations.
· Keep tracking of registration status, submissions, approval and registration timeline
· Establish strong relationships with appropriate regulatory reviewing bodies efficiently to facilitate the smooth registration activity
· Understand and practice on time the updates in regulations/new guidelines/circulars by DAV
· Co-ordinate with AbbVie in Artwork Label Reviewing and Approval process.
· Support to Marketing Team on internal reviewing/ submiting/geting approval for brochures
· Support to Tender Team on submiting/following/geting approval of Brand Name Listing, EU GMP Listing,
· Support to Tender team by checking tender dossier requirement, fulfil the required information and providing available documents for tenders, clear up the tender document s content.
Yêu cầu
Yêu Cầu Công Việc
1. Education & Qualification
Bachelors Degree in Pharmacy
Good relationship with the authorities related to registration tasks (Ministry of Health, Drug Administration of Vietnam)
Good knowledge and understanding of legal requirements related to product registration for pharmaceutical products
2. Working Experience
At least 5 years of managerial/specialist experience in Regulatory Affairs for the Pharmaceutical industry
3. Skills
Good command of English
Computer literacy
Good communication skills
Reporting skills
Problem-solving skills
Analytical skills
4. Other Specific Requirements
Careful
Honest
High sense of responsibility
Quyền lợi
Laptop
Chế độ bảo hiểm
Du Lịch
Chế độ thưởng
Chăm sóc sức khỏe
Đào tạo
Tăng lương
Thông tin khác
Địa điểm làm việc
Hà Nội
Sài Đồng, Long Biên, Hà Nội
Thông tin chung
Thu nhập: Cạnh tranh
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Tags:Tuyển dụng Hà Nội, việc làm Hà Nội, Công ty TNHH Zuellig Pharma Việt Nam tuyển nhân viên

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