北京招聘

Responsibilities/ Authorities工作职责权限:

·Providing professional knowledge and experience of pharmaceutical product registration within China and Asia Pacific region

·Establishing & tracking R&D registration projects, including schedule and action plan for new products or existing product changes;

·Working closely with project teams and other personnel to gather relevant information;

·Preparing and maintaining R&D related product registration dossiers complying with all Pharmaceutical (and medical devices) registration requirements;

·Coordinating and responding to requests for product registration related information;

·Communicating with other regulatory teams within different regions, such as Asia Pacific and the Hong Kong headquarters;

·Other related duties and tasks as required.

Qualifications: 任职资格

·Minimum Bachelor Degree in Pharmacy, Biomedical Science, or related degree;

·5 or more years of experience in regulatory affairs;

·Must have working knowledge of SFDA, GMP, FDA, ISO and related regulations;

·Good project management, problem solving and decision making skills;

·Fluent in both spoken and written English and Chinese;

·Excellent communication skills.

·Be comfortable working in a changing environment which requires flexibility and involves risk.

费森尤斯集团（德国）是一家全球性的医疗保健服务公司,以优质的医疗产品和可信赖的治疗服务享誉全球，是世界五百强企业之一。费森尤斯集团由位于全球范围内的四个独立的事业部组成，包括费森尤斯医疗用品、费森尤斯卡比、费森尤斯赫里奥斯、费森尤斯奥美德。
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