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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.
自免CMO将在零售行业的生命科学部门中负责战略规划、市场拓展和团队管理。候选人需要具备深厚的专业知识和卓越的领导能力,以推动组织的业务增长。
这个岗位主要负责公司的多肽和EK酶等相关项目的技术革新。
主要职责是领导和优化生产工艺,确保高效、安全和合规的生产流程。候选人需具备生命科学领域的专业背景及丰富的工艺管理经验。
病毒囊泡类负责人总监将领导相关领域的研究和开发工作,推动生命科学领域的技术创新。该职位需要候选人具备深厚的专业知识和卓越的领导能力。
生物制剂研究员/项目负责人将在生命科学领域中,负责生物制剂的研究与开发工作,推动项目顺利进行。此职位需要具备专业知识与实践经验,以确保研究项目的高效完成。
临床培训经理将在生命科学领域中负责开发、实施和优化临床培训计划,确保专业人员能够熟练掌握相关技能和知识。该职位需要在北京工作,适合有能力推动培训项目成功的候选人。
本职位负责海外药品注册工作,确保符合国际法规要求并推动产品顺利进入目标市场。我们正在寻找一位熟悉药品注册流程并具备卓越执行能力的专业人士。
作为RA总监,您将负责领导和管理注册事务团队,确保公司产品在国内外的注册和合规工作顺利进行。此职位需要在生命科学行业中展示卓越的战略规划和执行能力。
医学VP职位需要具备深厚的生命科学专业知识和战略领导能力,帮助企业推动医学项目的发展和执行。该岗位位于北京,适合热衷于生命科学行业的专业人士。
该岗位需统筹管理全球注册事务,协调跨部门资源,加速产品的国际化进程,同时建立和维护与各国监管机构的良好关系,提升企业在国际市场的合规运营能力。
The Drug Discovery Lead will be tasked with leading the development of operations in this exciting field and the development of a new drug discovery portfolio.
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