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.

This role leads the design, optimization and preclinical development of therapeutic peptides, PDCs and constrained macrocycles using structure-based and AI-driven drug design tools, while conducting SAR studies and cross-team collaboration to enhance candidate potency, druggability and binding performance.

这是一份激动人心的机会，作为一名早期研发科学家，您将负责推进生命科学领域的前沿研究项目。我们正在寻找一位能够通过创新和专业知识推动研发工作的专业人士。

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.

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。

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。

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.

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.

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。

Lead the development and validation of nutrition-related claims by transforming scientific evidence into consumer-relevant messaging aligned with business strategy.

Partner closely with marketing, regulatory, and R&D teams to ensure all communication is scientifically sound and compliant with local requirements.

The role blends global technical leadership with local China accountability, acting as the single medical science point of contact for Greater China and the face of medical science to internal stakeholders, partners and external bodies.

The successful candidate will drive medical science-led innovation, evidence generation and commercial alignment, balancing scientific rigor, regulatory compliance and business growth across a diverse portfolio.

担任整个国际化注册项目的负责人

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.

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.

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。