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。
担任整个国际化注册项目的负责人
This role oversees end-to-end regulatory affairs for the China business: market entry, standards and labeling, claims and packaging compliance, risk identification and response, and professional engagement with authorities and industry bodies. It requires managing multiple projects in a fast-paced, results-oriented environment and partnering with R&D, FSQ, Marketing, Legal and Supply Chain to secure compliance across the product lifecycle.
As RAQA Manager, you will be responsible for driving the regulatory and quality strategy for China registration of a Class II active medical device. You will collaborate closely with cross-functional teams and external stakeholders to ensure timely and compliant market entry.
This role focuses on regulatory compliance for Third-Party Manufacturing (TPM) projects, ensuring raw materials and formulas meet all applicable standards. It requires strong communication skills to coordinate with R&D teams, TPM suppliers, and global regulatory counterparts, while optimizing processes for efficiency.
This role is responsible for managing regulatory-related activities in China to support business operations and mitigate uncertainties. It plays a critical role in ensuring regulatory compliance for product importation into the Chinese market and actively participates in market-related activities, including compliance assurance and crisis management from a regulatory affairs perspective.
The Global Regulatory Affairs function maximizes opportunity & minimizes risk by guiding business decisions based on scientific & regulatory insight to ensure the freedom to launch these new innovations.The Regulatory Manager will develop and implement the regulatory strategy for novel ingredients and products to ensure successful and timely launch in APAC markets.
The Head of APAC Regulatory Affairs leads the APAC Regulatory Team and work collaboratively with cross functional partners to support the company's regional and global objectives by enabling continuous market access of the existing portfolio and innovations.
Lead the development and execution of China region regulatory compliance initiatives, annual plan and budget, relevant company Standards compliance and audits, submit documents and reports into systems and global RA function, and related issues management. This position also acts proactively and strategically, identifies potential regulatory issues and trends, develop strategies, drive effective approach and advocacy.
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.
资深塑胶/电子报价专家负责为塑胶和电子产品提供专业的报价分析与支持，确保公司在快速消费品行业中的财务运营高效且具有竞争力。此职位位于东莞，适合擅长财务分析和成本控制的专业人士。
The role will play a key role in bridging business needs with technology solutions, supporting the life science industry. Based in Shanghai - Huangpu, this role focuses on enabling strategic initiatives through effective collaboration and technical expertise.
This role goes beyond traditional quality leadership. We are looking for a senior executive who can translate technical quality and regulatory requirements into commercial value, supporting business growth while maintaining the standards of compliance and food safety
Lead consumer technical insight activities in China, translating consumer understanding into product design, innovation pipeline and performance evaluation.Act as a key bridge between market, R&D and marketing teams to ensure products meet real consumer expectations and business objectives.
负责建立和持续优化产品工业化生产技术体系，实现实验室成果向稳定量产的高效转化，同时确保产品营养、风味及品质表现的一致性。领导工艺开发、技术创新、设备适配及生产优化工作，推动生产效率提升、质量稳定及成本改善，支撑企业长期业务发展。
Create Job alert to receive 生命科学 生命科学 法规事务 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.
