一、Job description ? Responsible for regulatory tasks in medicine category under business unit of Reckitt. 1）Lead regulatory processes of medicine projects to ensure timely filing, approval of new registrations in accordance with business objectives. 2）Follows up relentlessly with global functions including GRA, Medical, RD and QA group for supports to enable local projects smooth. 3）To assist in championing procedures to expedite commercialization of new OTC products and business strategy. 4）Builds relationships and negotiates with local regulatory agencies on all matters relating to medicines development, compliance and safety in local market 5）Keeps abreast of regulatory changes and communicates aggressively to management team, global regulatory, medical and marketing groups. 6）Establishes strong working relationships with Reckitt & Manon agencies, customers and business colleagues, provide supports and guidance to ensure all efforts focused on successful commercialization of medicine. 二、Requirement 1）Education: Bachelor degree and above, major in medicine, biochemistry or other related major; 2）Work experience: 5-8 years and above working experience in medicine regulations, familiar with relevant laws and regulations of industry; end to end regulatory project experience, medicine product experience is preferred; 3）Strong communication and coordination ability and sense of responsibility, good team spirit; 4）Language and skills: good English listening, speaking, reading and writing; Proficient in office software; 5）Core quality: responsible & reliable, detail oriented, able to work under pressure.