Regulatory Affairs Executive

Req ID: R0023101
Category: Contractor
Location: Hanoi, Ha Noi VN

Posted Date: May 22, 2018

• Identify and compile regulatory documents for submission according to local requirements, including for medical devices registration.
• Providing support for online submission of registration dossiers.
• Be an operator for physical submissions of dossiers the the health authorities.
• Support other general activities to Vietnam RA/QA manager to ensure timely and compliant submissions
• Assist in preparation and review of labeling, SOP’s, and other departmental documents
• Maintain regulatory files in a format consistent with requirements
• Daily administrative works that include filing, keeping and maintaining records required for smooth operation of regulatory functions