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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.
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。
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。
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.
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.
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。
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。
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.
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。
The Global Director, Quality Assurance & Regulatory Affairs will lead the company's global QARA function, overseeing quality systems, regulatory compliance, audits, supplier quality, and market access activities across international markets. This role will manage a team of QA and RA professionals while collaborating with cross-functional stakeholders, external regulatory bodies, notified bodies, distributors, and regional regulatory partners worldwide.
负责蛋白表达平台的生产运营与团队管理,统筹外部客户订单交付,持续优化生产工艺,保障质量、产能及交付效率。
The Tissue Culture Lab Manager will oversee the end-to-end operation of a plant tissue culture laboratory, ensuring high-quality, efficient, and compliant production of tissue culture plantlets. The role will lead technical optimization, team management, laboratory safety, and cross-functional collaboration to deliver propagation projects at commercial scale.
我们正在为一家全球知名欧洲创新医药企业寻找一位 HR Shared Services Coordinator。该岗位将加入亚太区HR Shared Services团队,负责员工全生命周期相关的人力资源运营支持,并作为员工与HR团队之间的重要桥梁,提供高效、专业的人力资源服务。
RNA药物成药性评估、递送体系理解以及IND申报经验
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.
创建职位提醒,一旦有新的全国 生命科学相关职位发布,您将第一时间通过电子邮件收到通知。
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