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You will lead a project team and be responsible for the medical device business landing and launching program in China market from regulatory, safety, claims aspects.
The China Regulatory Affairs Manager will provide leadership and strategic direction for the Regulatory department in China. They will ensure that all local regulatory requirements are met throughout product lifecyle, from guiding formula development and innovation, to reviewing marketing/advertising materials such as labels and securing advertising permits, to handling post-launch reporting.
Est.1981, mature enterprise who delicate into the bee product head down;Servicing domestic and international clients with various products covering food&beverage, personal care, health & nutrition, animal care, and different types of OEM/ODM depending on requests
Full cycle Regulatory Affairs support from plant to end product;Provide RA advice for NPD;Cross function prepare related documents including but not limited to labels and raw material list;
Report to the Board, comprehensively preside over the daily operation and management of the company. Achieve the company's listing goal.
As China RA Head, report Global senior RA VP, work with global team to get involved in compound development strategy, clinical development strategy and RA strategy.
As RA Head, responsible for full RA job from strategy to project operation.
Managing complete drug variations
注册副总监负责产品的中美双报。
注册总监,直接汇报给公司CEO,带领注册团队完成国内国际注册。
作为集团注册总监,负责组建注册团队;负责与各大型检测机构,第三方合作公司,以及国家注册局方等保持紧密的沟通和合作;建立注册平台统筹资源,对内赋能,对外资源对接。
规划管理公司产品注册相关工作负责评估和制定适合企业长期发展的知识产权保护策略
工作地点在北京国贸地区。汇报给公司的CMO,注册总监要负责带领北京和成都的注册团队负责产品的NDA。
负责公司油脂类产品业务相关的法规事务,产品注册,内外部法规支持。
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。
新产品注册
负责法规事务的操作,确保产品注册并执行法规事务活动,管理和协调产品注册及注册团队
负责内分泌领域药品相关国内注册工作。
My client is a market leader with their Orthopedic Device Products with expansion plans in Asia. We are hiring a Team Head position in Asia to be responsible for Regulatory Affairs and Quality Management.
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。
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