26/06/2024
Nhân viên chính thức
Cạnh tranh
Mới tốt nghiệp
30/06/2024
RESPONSIBILITIES
1. Support all RA processes to ensure compliance:
Support Product Notification process for NPL (New product launch) & EPL (Exist product launch) by :
o Check ingredients to ensure the compliance of formula.
o Prepare dossiers for notification submission & obtain notification approval and filing the Master Notification file.
o Collect data from Regone/PDS and share to agency for notification preparation & submission.
o Follow up closely with Drug Administration Vietnam (DAV) to update status of submitted notification.
o Update final name on CFS to master file.
o Request CFS & LOA for products.
o Check all data of products in RegOne /PDS/RDS systems and upload data to Regone systems.
o Manage product data in system, processing file, master file,…
Support Advertising License process:
o Prepare all advertising documents & submit to Department of Health HCM (DOH HCM).
o Follow up with DOH HCM to update status of submission.
Support Vietnamese labelling:
o Check & update new Vietnamese labelling to master file.
o Request APAC to create new content labelling (if any).
2. Administration tasks:
o Proceed payment to DAV and agency.
o Follow up with those Authority to collect invoices.
3. Other tasks: as assigned by line manager.
▪ Regulatory Affair experience 1-2 years.
▪ University Degree or College Degree with major Biology Technology/ Chemical/ or relevant major.
▪ Good-looking appearance.
▪ Good in English (written & speaking).
▪ Good communication skills, written and verbal.
▪ Good organizational skills, time management and follow up skills.
▪ Able to prioritize and handle several tasks simultaneously.
▪ Excellent Computer office skills. (excel)
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