Legal jobs in China

This role is responsible for ensuring compliance with global export control regulations and customs requirements, while supporting business operations across China through risk management and regulatory guidance. The position also involves cross-functional collaboration, audit and licensing support, and driving process improvements to enhance trade compliance effectiveness and efficiency.

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.

• This role contributes to business ethics and legal compliance by handling case management, legal research, project coordination, internal training materials, policy guidance, and translation under attorney supervision.

与产研团队一起，从专利撰写、申请、答复、布局等角度与AI结合，优化AI产品

US IPO Associate.

岗位定位全面负责量化私募证券基金的合规与风控管理，统筹内控体系建设及监管事务

作为MP米高蒲志上海财务/法务团队的一员，你将深度参与中国区财务战投/法务中高管人才市场，服务世界知名跨国公司、行业头部企业与快速增长的本土独角兽。你不仅是招聘顾问，更是业务伙伴与专业领域专家。

• 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。

该职位适合一位具有PEVC经验的2-3年级律师，能够在专业服务行业中提供高质量的法律支持，同时处理复杂案件。工作地点在上海，要求候选人有较强的专业能力和出色的团队合作精神。

作为董事会秘书，您将主要负责支持公司治理事务和董事会运作，高效对接监管机构、审慎应对资本市场问询，并在公司治理优化过程中发挥关键稳定作用。

作为合规一号位，带领团队支持中国区全盘合规工作。

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.

担任整个国际化注册项目的负责人

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.