Tuyển Regulatory Affairs Executive

• 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.