Legal jobs in China

• 全面负责公司法律事务管理，搭建并完善跨境业务合规管理体系，覆盖跨境运营、红人营销合作、产品标签合规、数据安全与个人信息保护等核心领域，确保业务全流程符合国内外相关法律法规及监管要求。

新增法务负责人岗位，支持公司上市，分管法务及知产。

硬件法务负责人负责管理与硬件相关的所有法律事务，确保公司运营符合法律法规。该职位需要熟悉法律条款及其在实际业务中的应用。

我们正在为一家业务稳健的新能源企业寻找一位法律合规中心总经理，该公司在风电、光伏等清洁能源领域深耕多年，项目遍布全国，业务规模持续扩张，行业地位稳健。

A股上市，全球业务布局，业务高速发展

法务负责人，构建并领导全球化法律合规体系，支持海外业务战略落地，规避国际业务中的法律风险​

作为合规风控，负责支持基金的募投管退过程中的合规，及基金运营合规。

Role snapshot

As the Head of Compliance for our China entity, you will act simultaneously as strategic radar and execution engine-anticipating regulatory shifts before they happen and embedding policies, processes, tools and culture that let the business scale confi-dently and compliantly.

您将负责全球数据合规，并深度参与公司整体合规治理体系的建设与运营。

The APAC Compliance Head will oversee compliance functions within the business services industry, ensuring adherence to regional and global regulations.

• 负责公司合规体系建设与维护，跟踪法规变化，识别并防控合规风险，审核业务流程，组织培训，协助应对监管检查，确保企业运营合法合规。

US IPO Associate.

作为一名交易&基金组律师（2-5年级），需要具备基金募资/设立与 PE/VC 投资交易的实操经验，同时需要强执行力、良好沟通能力与长期深耕基金与股权交易业务的意愿。

This role leads global patent strategy and portfolio management across major jurisdictions (US, EU, Japan, Korea, China) to protect biotech innovations.

You will build an in-house IP team and support high-value transactions and commercialization.

贸易合规总监将负责制定和执行反垄断合规策略，确保企业在相关法律框架内运营。

该岗位负责证券公司二级市场业务的合规审查、咨询、培训、检查等工作，要求具备相关专业背景、7 年以上相关经验（含二级市场合规管理经验）、扎实专业能力及流利英语水平。

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.

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.

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.