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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.
The Head QA/QC - Baby Goods will oversee quality assurance and control processes within the engineering and manufacturing department of an FMCG company. This permanent role, based in Dongguan, requires expertise in maintaining high standards for baby goods production.
Overall business management, focusing on operational performance, commercial growth, and organisational development within a manufacturing environment.
作为公司半导体器件质量的技术权威，您将负责对中国本土供应商的CPU、MCU、存储器（Flash,DRAM, SRAM 等）、FPGA 等核心逻辑半导体器件进行全面的质量评价、风险鉴定与供应商管理。您的专业知识将直接指导研发团队正确选型与应用，有效识别并管控潜在风险，确保产品的功能、性能、质量与可靠性满足中国客户的需求。
A management role aiming for driving automation strategy, standardisation, and deployment across manufacturing sites, ensuring efficient and scalable production performance from initial design through ramp-up.
该岗位负责储能产品强电系统及关键部件的质量管理，建立并优化供应商质量体系，确保产品可靠性、合规性及供应链质量稳定。你将主导供应商质量改善和技术问题闭环，与研发、采购及制造团队密切协作，持续提升产品质量水平和供应链竞争力。
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