Browse our jobs and apply for your next role.
The right candidate is just a few clicks away
PageGroup changes lives for people through creating opportunity to reach potential.
If you have any questions, we’re here to help.
Looking for junior candidate with 3 years of experience who can grow with the team
Looking for Mid-level Regulatory Compliance candidate responsible for HKMA and General Compliance matters.
执行公司质量方针政策,组织分解和实现质量目标。完善符合中国和欧美GMP的质量管理体系,确保质量管理体系在法律法规要求下高效运行。负责各部门GMP指导、监督、检查,提高全员GMP意识。履行质量管理负责人、质量受权人及产品放行人职责,对公司药品和保健食品产品质量负责。负责产品全生产周期质量管理。推进产品国际化认证工作。
总部在山东的大型民营医疗器械集团诚招一名高级合规经理。
As the China Regulatory Affairs Manager, you will oversee regulatory projects for China, you will be a part of a growing team, interacting with other departments.As a member of the Regulatory Affairs Department, you will implement and lead regulatory projects to ensure compliance with the various regulations related to food and food supplements, electronic devices, and cosmetics.
1.Provide End to End regulatory expertise to innovation projects in China R&D.2.Ensuring compliance of raw materials and finished cosmetic products developed in line with chemical and cosmetic regulations in China and Asian countries.
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.
Lead and manage a regulatory affairs team, providing guidance and oversight for regulatory compliance and food safety.
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.
A reputable international law firm is looking for a mid or senior level Corporate Associate to join their Beijing office.
overseas law firm is now looking for office manager to take over shanghai office daily operation management, legal sec team management and other partner assigning work. our client is the typical overseas law firm working environment with stable business status in China market.
作为知识产权(专利)方向的负责人,主要负责公司专利布局和分析,带一个小团队
This role will direct report to compliance head based in APAC. This role will provide leadership and execution in the deployment of the Compliance program to drive the business.
This is an excellent opportunity for aviation lawyers to join in-house to further progress his or her career in a regional role. Candidates who are currently outside of Hong Kong are also welcomed to apply.