Responsibilities:

• Ensure drug registration activities are proceeded in accordance with relevant local, mainland China and overseas regulations and develop the strategy to obtain the product approval within target timeframe;
• Provide overall regulatory guidance towards execution;
• Monitor and communicate within the company for the current and proposed changes on drug registration dossiers to ensure all the operations within company relating to product registration comply with the regulatory requirements and business needs;
• Supervise and monitor all supporting activities relating to drug regulatory requirements are proceeded according to schedule.

Requirements:

• University graduate major in Science or medical related discipline;
• 8 years regulatory affairs experience in pharmaceutical industry is preferred;
• Good working knowledge and experience on local, mainland China and overseas drug regulatory requirements;
• Strong interpersonal and communication skills;
• Detail-oriented and cross-functional team player;
• Proficiency in written and spoken English & Chinese including Mandarin.

Interested parties please send full resume with present and expected salary to Human Resources Department by clicking "APPLY NOW".

(Information provided will be treated in strict confidence and will only be used for recruitment-related purposes.)