China jobs in Life Sciences

This role is responsible for developing and implementing China-focused early clinical development strategies to generate high-quality, decision-driving data for global programs across genetic neurological, renal, pulmonary, and other rare genetic diseases.

负责制定和推动公司全球注册战略，统筹创新药、高端仿制药及生物药在中国、欧美等国际市场的注册申报、监管沟通及药政体系建设，支持产品全球上市

作为一名临床前 Dmpk / 毒代科学家，您将负责支持生命科学领域的药物研发工作，专注于药物代谢和药代动力学研究，为新药开发提供科学支持。

作为一名临床前PK/药效学（PD）科学家，您将负责支持药物研发项目的药理学和药效学研究工作。这一职位需要您在生命科学领域展现专业技能，推动项目进展。

知名MNC平台，深度参与创新药从研发到临床转化的关键节点。

国际注册总监负责制定并执行公司药品/生物制品全球注册战略，主导FDA、EMA等重点市场的注册申报与法规合规管理，推动产品高效获得国际上市批准。

The Medical Advisor will play a crucial role in providing medical and scientific expertise within the life sciences industry. Based in Beijing, this position involves supporting medical strategies and ensuring compliance with medical guidelines and regulations.

The Medical Advisor role in the Life Science industry requires a professional with expertise in medical strategy and scientific communication.

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.

We are looking for an experienced CMO to lead the medical strategy and clinical development of our stem cell and regenerative medicine portfolio.

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.

An exciting National Medical leadership opportunity for an experienced Medical Affairs professional to drive scientific exchange and stakeholder engagement across China. The role offers significant autonomy, exposure to senior leadership, and the chance to contribute to the future growth of the Medical Affairs organization.

高级项目经理需要在上海的生命科学行业中担任重要角色，负责销售部门的项目管理工作。理想的候选人需要具备优秀的项目管理能力和相关技能，能够推动项目顺利进行并实现目标。

医疗总监负责在生命科学领域内领导和管理医学事务，确保公司目标与行业标准的紧密对接。该职位位于北京，要求候选人具备深厚的医学知识和卓越的领导能力。

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.

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

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.

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.

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.