浏览我们的职位并开启您的下一步申请
只需点击几下,即可找到合适的候选人。
PageGroup通过创造挖掘潜能,让您绽放自我,成就精彩人生
如果您有任何问题,我们很乐意为您提供帮助。
搭建企业内控合规体系管理法务团队
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.
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
Create Job alert to receive Legal 生命科学 jobs via email the minute they become available
Submit your CV to register with us and we will contact you if a suitable role becomes available.