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Typical Accountabilities ? Implement regulatory strategies to achieve in-time and high quality approval and facilitate full speed launch. ? Maintain product licenses through timely lifecycle management with high standard. ? Effectively manage the local and global regulatory support systems/information to ensure good coordination for all stakeholders. ? Establish relationship with local regulatory authorities with the guidance of senior regulatory manager. ? Monitor local regulatory environments and communicate to key stakeholders, support to exert regulatory influence through company initiatives and/or industry association joint forces. ? Adherence to AZ and industry code of conduct, ethics and good regulatory practices including AZC RA SOPs and other required SOPs. Education, Qualifications, Skills and Experience Academic / Professional Qualification x Bachelor degree or above in Pharmacy, Medical, Biology or related field. Technical / Skills Training pharmaceutical company. x Understand the current regulatory practices and regulation in China. x Strong collaboration across teams. x Good project management skill. x Fluent in both oral and written English. x Good computer skill: word, excel, power point. Working Experience x Minimum 2 years’ experience in below position. x Minimum 4 years working experience in regulatory affairs of MNC Pharma Company.