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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.
RNA药物成药性评估、递送体系理解以及IND申报经验
The Global Regulatory Affairs function maximizes opportunity & minimizes risk by guiding business decisions based on scientific & regulatory insight to ensure the freedom to launch these new innovations.The Regulatory Manager will develop and implement the regulatory strategy for novel ingredients and products to ensure successful and timely launch in APAC markets.
The Head of APAC Regulatory Affairs leads the APAC Regulatory Team and work collaboratively with cross functional partners to support the company's regional and global objectives by enabling continuous market access of the existing portfolio and innovations.
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.
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.
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。
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。
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。
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。
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。
Join a global pharmaceutical organization to originate and drive high-value biosimilar licensing and partnership opportunities across APAC, supporting the expansion of its global biosimilars portfolio.
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。
As a key member of the executive management team (CEO/General Manager), you will take full responsibility for overall business operations and lead the company through the critical transition from product registration to launch and commercial execution.
- Develop and implement the overall business strategy in Australia, aligning with the overseas Business objectives and local market dynamics- Provide visionary leadership to drive the achievement of revenue targets, market share growth, and profitability
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。
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。
从零搭建完整医学事务体系,覆盖上市前研究、上市后支持及医学传播全链路。以业务结果为导向,构建"证据+专家+传播"的医学能力,直接参与商业落地。
该岗位为研发(RD)团队助理岗位,将支持中国营养与科研团队的日常研究及专业支持工作。岗位内容兼具科学研究支持 + 市场信息分析 + 合规审核,适合具有营养/食品科学背景,希望向科研或科学事务方向发展的候选人
本地化运营支持经理将主要负责拉美地区的相关工作,重点是支持生命科学领域的本地化运营和协调。该职位需要具备强大的跨文化沟通能力和丰富的运营管理经验。
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