China jobs in Life Sciences

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.

肿瘤领域CMO负责推动肿瘤领域项目的临床开发和实施，确保项目符合行业标准并取得成功。您将与研发团队紧密合作，制定战略并监督执行，以推动关键项目的进展。

高级生物信息分析师将负责生命科学领域的数据分析和解读，支持业务服务行业的研究和开发。此职位要求候选人具备扎实的专业知识和分析能力，以提供高质量的解决方案。

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.

The position of R&D Data & AI in Chemistry within the life sciences department requires expertise in data-driven methodologies and artificial intelligence applications. The role is based in Brentford and focuses on leveraging technology to enhance research and development processes in the business services industry.

The Medical Director China will be responsible for incorporating and executing the local medical plan developed from the Global Medical and Marketing Strategical Plan incorporating local market and medical insights. This person will be accountable for Medical Governance and the medical ethical standards within the Country Organisation and takes full responsibility for the medical management in China - drives and leads all medical activities.

Translate complex scientific concepts into clear, credible brand narratives, strengthen collaborations with dermatology experts and scientific communities, and adapt global scientific storytelling for the Chinese market.

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 permanent role in the life science industry is focused on transaction services within the investment department, requiring expertise in accounting and finance. Based in Shanghai, this position offers a competitive salary and the opportunity to work on impactful financial operations.

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.

作为医疗经理，您将负责在快速消费品行业中支持与生命科学相关的项目管理和执行，为公司业务目标的实现提供专业的医学支持。该职位要求候选人具备医学领域的专业知识，并能在北京地区高效开展工作。

生物制剂研究员/项目负责人将在生命科学领域中，负责生物制剂的研究与开发工作，推动项目顺利进行。此职位需要具备专业知识与实践经验，以确保研究项目的高效完成。

Oversee product design and development for gummies and similar products to drive growth, focusing on China and other Asia regional 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.

器械营销总监负责制定和实施销售战略，推动公司在生命科学领域的市场份额增长。此岗位需要具备卓越的销售管理能力以及对生命科学行业的深入了解。

中成药医学负责人将负责公司中成药产品的医学策略制定和实施，确保相关产品符合行业标准并支持市场需求。该职位要求候选人具备扎实的中医药知识及医学专业背景，能够推动产品的医学价值。

抗体研发项目总监负责生命科学领域的研发项目管理，确保项目按时、高质量完成。此职位需要具备丰富的专业知识，并能够高效协调团队资源，推动项目成功实施。

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。

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.