生命科学 jobs in China

Take Global R&D platform leadership and lead core strategic projects to be landed globally.
Deliver key technical insight capability to team and projects.

The Evaluation Manager at our skin care cosmetics company is a key contributor to both innovation and launched projects. This role is responsible for providing crucial support for skin care claims through consumer testing and sensory evaluation. Reporting directly to the global R&D department, the Evaluation Manager will closely collaborate with both global and local R&D teams to ensure product excellence and market success.

临床医学经理-呼吸负责支持呼吸领域的临床项目，通过协调与管理确保项目的高效开展。我们正在寻找一位能够提供专业医学支持并协助项目成功的候选人。

该职位负责制定和实施全球临床开发战略，确保产品开发符合行业标准和法规要求。候选人将与跨职能团队密切合作，推动生命科学领域的创新与发展。

临床医学SD-ED负责支持临床研究项目的设计、实施和管理，确保项目符合科学和法规要求。该职位适合对生命科学领域有深入了解并希望在临床研究中发挥重要作用的专业人士。

临床药理职位负责支持药物研发中的临床药理学研究工作，确保研究的科学性和合规性。该职位需要具有扎实的生命科学背景，并能够有效地与跨部门团队协作。

担任整个国际化注册项目的负责人

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.

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.

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.

研发总监负责领导生命科学领域的研发工作，确保项目的高效推进和技术创新。理想的候选人需具备深厚的专业知识和管理能力，能够带领团队实现目标。

药化VP负责领导药物化学团队，推动创新药物的研发项目。该职位要求具备深厚的药物化学专业知识和卓越的领导能力。

药化总监将在零售行业的生命科学部门中，领导团队进行药物化学研发工作，推动项目从研发到实施的高效转化。此职位需要具备深厚的药物化学知识及项目管理能力，确保研究成果符合行业标准。

生物首席科学家将负责生命科学领域的研究与开发，推动零售行业内的技术革新和产品优化。您将带领团队完成科学研究项目并支持公司的战略目标。

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.