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知名MNC平台专注CTA方向发展，深度参与创新药从研发到临床转化的关键节点。岗位为1年contractor形式开始，长期续签
Lead regulatory affairs activities for Thailand operations and support market access, product compliance, and registration activities across key ASEAN markets.Serve as the regional regulatory expert, providing strategic guidance on formulations, ingredients, claims, labeling, and regulatory pathways for both local and export markets.
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.
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 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.
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.
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.
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.
An Audit Manager is required in Shanghai to oversee and enhance the internal audit processes within the industrial and manufacturing sector. The role focuses on ensuring compliance, risk management, and operational efficiency.
We are seeking a Finance Accountant to support the financial operations within the industrial/manufacturing sector in Shanghai. The role involves managing financial records, ensuring compliance, and contributing to efficient financial processes.
我们正在寻找一位结构设计工程师，参与创新型可穿戴电子产品的结构研发工作。该岗位将负责产品结构设计、可靠性验证及量产导入，推动产品从概念设计到规模化生产落地。
The Corporate Strategy and Business Intelligence role in the life science industry involves shaping strategic goals and providing actionable insights to support business growth. Based in Shanghai, this position is ideal for individuals with a keen interest in consultancy, strategy, and change management.
汇报给投融资总监，负责公司投资者关系及融资工作，搭建资本市场生态，推动股权融资项目落地并提升公司资本市场影响力。
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