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负责内分泌领域药品相关国内注册工作。
负责所承担项目的临床药理学和/或定量药理学研究/设计临床药理学研究并撰写I期研究方案和总结报告/与医学团队、早研团队等一起在项目组里推进临床项目。
质量副总经理隶属公司总经理直接领导,对总经理负责,向总经理报告工作。分管公司质量管理部;质量副总经理为公司的质量负责人,具有质量否决权。负责根据公司质量目标组织建立公司年度质量计划,负责为实现质量目标所涉及的各项工作提供支持;
根据公司立项和研发计划,制定公司产品注册年度计划并组织实施,主导整个申报注册过程,根据蕞新适用的法规,独立编制IND、NDA及变更等各类提交文件,跟踪项目审评审批及检验进度。
根据公司产品规划,安排注册进度,负责督导产品注册全过程 ,负责起草、编制标准化文件,确认并提交注册申请。
公司目前为了大规模生产,要在北京建设一个全新的工厂包括原液和制剂,2-3条2000升的产线,产品全球卖。目前公司诚聘生产副总裁,负责建设和管理新的工厂,同时管理目前的两家工厂,团队共计200人。
中国区RA HEAD负责整个国内的注册策略制定,团队的搭建,以及管线产品的注册。
The job holder is responsible for the development of our client's operations in China. Key task areas will include but are not limited to market share improvement, financial performance, personnel development, physical asset management etc.This job is also open to expats who has solid working experience in China.
Report to the Board, comprehensively preside over the daily operation and management of the company. Achieve the company's listing goal.
Our client is a Family Business in Europe with Global Headquarter in China. Due to their business strategy change plus their full commitment in China, they are now looking for a Global CEO to join the organisation to oversee a 400 Million Euro business with around 3000 employees globally.
This role is China Head of Operation, directly report to China president. In charge of multiple plant operation management in China mainland.
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