Legal职位 - 中国地区

• 负责公司合规体系建设与优化，统筹制度管理、风险评估、合规培训及内控协同，保障公司治理及经营活动合规开展。

作为律所的行政前台，你将全面负责前台接待、访客引导与会议活动支持，在上海陆家嘴高端办公环境中与办公室经理紧密协作，成为这家全球知名律所日常运营的重要窗口。

• 负责公司法律合规体系建设与法律风险管控，为业务运营、战略决策、产品服务上线及对外合作提供全流程法律支持。
• 统筹合同管理、知识产权保护、争议解决及合规培训等工作，保障公司经营合法合规并降低法律风险。

• 此职位位于上海浦西，直接汇报给区域法总。
• 需要具备医药行业合规相关的专业知识和技能，包括但不限于合规体系的搭建。

本职位主要负责生命科学领域的贸易合规事务，确保公司业务符合相关法律法规，并提供专业的法律支持和指导。工作地点位于上海，适合有相关领域经验并希望在法律部门进一步发展的专业人士。

This role serves as a trusted Compliance Officer, driving a proactive compliance culture while supporting business growth across a dynamic and fast-evolving healthcare environment.

Partnering closely with commercial, e-commerce, retail, marketing, and leadership teams to support sustainable growth while effectively managing legal and regulatory risks.

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。

作为知识产权领域核心负责人，深度参与对外合作、技术引进及授权交易，并推动公司知识产权体系建设与跨部门协同，助力企业创新成果的全球化保护与价值实现。

作为专利律师，您将负责国内及涉外专利申请、复审、无效及争议解决等全流程法律服务，并为客户提供专利布局与知识产权战略支持。该岗位面向具备电子或生化技术背景的人才，能够充分发挥技术与法律复合型专业优势，服务创新型企业及行业知名客户。

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。

作为 360° 专业招聘顾问，你将成为客户与候选人之间的核心桥梁，提供真正有价值的商业咨询服务，而非简单的"人才匹配"。

• 清晰的职业发展之路
• 良好的团队协作文化

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.

The Global Director, Quality Assurance & Regulatory Affairs will lead the company's global QARA function, overseeing quality systems, regulatory compliance, audits, supplier quality, and market access activities across international markets. This role will manage a team of QA and RA professionals while collaborating with cross-functional stakeholders, external regulatory bodies, notified bodies, distributors, and regional regulatory partners worldwide.

The Regulatory Affairs Manager will lead regulatory activities in China, ensuring product compliance, registration execution, and effective engagement with regulatory authorities and external partners.

This role serves as a key business partner to commercial, quality, innovation, supply chain, and global regulatory teams, supporting market access and long-term portfolio growth.

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.

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.

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.