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负责制定并领导公司创新药管线的临床开发战略,推动项目从IND申报、早期临床研究到关键开发阶段,并带领团队实现全球临床开发目标。
Join an innovative biotech to lead early clinical development across a growing Immunology & Inflammation pipeline, with responsibility spanning Phase 1/2 strategy, study design, medical oversight and clinical decision-making.
Play a key role in the design and optimization of therapeutic peptides, peptide-drug conjugates (PDCs), and macrocyclic molecules. Work closely with our US-based scientific leadership and cross-functional discovery teams to translate innovative ideas into high-quality intellectual property and pipeline assets.
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.
作为集团首席科学官,负责统筹多个研发平台及研究院的科学战略、技术决策与创新协同,通过科学领导力推动组织共识形成、资源优化配置及创新研发体系持续升级。
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.
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。
We are looking for an experienced discovery professional combining scientific depth, innovative thinking and team leadership to build drug discovery capabilities from the ground up, advance programs from scientific concepts to PCC/IND, and explore the application of AI and emerging modalities in innovative drug discovery.
Join a rapidly expanding biotech as CSO, advanced scientific innovation from target identification through preclinical development while building a differentiated pipeline in oncology and immunology. We are looking for an industry-proven scientific executive with strong portfolio evaluation and drug discovery experience.
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.
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.
负责支持蛋白纯化技术的转移与优化工作,确保技术转移过程的顺利进行。该职位要求在生命科学领域具备扎实的专业知识和实际操作能力。
将负责在生命科学领域支持技术转移和工艺优化,主要专注于微生物发酵技术的开发和实施。
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.
小核酸事业部负责人将在杭州领导生命科学领域的核心业务发展,推动团队实现战略目标并在行业内取得更大突破。此职位要求具备丰富的管理经验和对小核酸技术的深刻理解。
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