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This position focuses on managing regulatory affairs for FSMP (Food for Special Medical Purpose) products in China. The role ensures timely registration, compliance, and strategic regulatory planning without direct team management responsibilities.
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.
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 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.
负责集团运营与产能管理建立分级标准与检测流程，维护质量体系
混合键合工程师负责为半导体行业提供高质量的技术支持和客户服务。该职位要求候选人具备相关的技术背景以及良好的沟通能力，以确保满足客户需求。
The Plant director role is an excellent opportunity to manage the operations of a manufacturing facility within the FMCG industry. Based in Beijing, this role requires a capable ownership to oversee production, efficiency, and quality control.
This role partners with overseas third-party manufacturers and internal teams-including Product Development, Supply Chain, Regulatory, QA, Clinical, Safety, and Packaging-to ensure timely, high-quality delivery of new product development projects. It also drives innovation by leveraging consumer insights and vendor capabilities to support business growth.
The KA Manager will manage key accounts and develop long-term relationships with clients within the transport and distribution industry. This role requires expertise in engineering and manufacturing to ensure the successful delivery of tailored solutions.
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