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drive and implement the registration strategies and plans to ensure earliest regulatory approval of new products;Oversees the regulation process for products requiring governmental approval, including filing necessary applications and handling all government interactions. Coordinates inspection of the organization and contract facilities, and develops procedures to ensure regulatory compliance. Ensures that project/department milestones/goals are met and adhering to approved budgets.任職資格：Bachelor degree above in science or health related discipline (Advanced degree PhD, MD, MS, PharmD preferred)With 5+ years of relevant regulatory affairs experience with broad knowledge of the pharmaceutical industry. Demonstrated ability to contribute to a continuous learning and process improvement environment.Have excellent knowledge of local regulatory system, needs to provide clear guidance and strategy to the teamStrong interpersonal skills with the ability to influence others in a positive and effective mannerHighly influential with the CFDAStrong team playerStrong sense of urgencyExcellent communication skills; both oral and written公司介紹：As a leading global player in specialty, branded and generic pharmaceuticals, has an extensive basket of products that provide treatment for a broad spectrum of acute and chronic conditions experienced through all stages of life. The Group continues to increase the number of lives benefitting from its products, reaching more than 150 countries. In line with the Group’s commercial, production and territorial strategies, has identified thrombosis, anaesthetics, high potency & cytotoxics and infant nutritionals as four therapeutic categories which will get the highest focus based on materiality and future potential.

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