Life Sciences职位招聘信息

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。

Take Global R&D platform leadership and lead core strategic projects to be landed globally.
Deliver key technical insight capability to team and projects.

The Evaluation Manager at our skin care cosmetics company is a key contributor to both innovation and launched projects. This role is responsible for providing crucial support for skin care claims through consumer testing and sensory evaluation. Reporting directly to the global R&D department, the Evaluation Manager will closely collaborate with both global and local R&D teams to ensure product excellence and market success.

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。

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 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.

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.

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。

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。

This is an exciting opportunity for an experienced professional to join the C-Suite of an innovative biotech start up. The role requires strategic leadership and operational expertise to drive the company's continued growth and success and clinical pipeline progress in China.

We are looking for an exceptional C Level talent with expertise in global IVD industry to lead an innovative start up organisation. In this role you will lead all aspects from R&D to Commercialisation and work closely with the Company Board.

This is an exciting opportunity for an independent commissioner to provide strategic guidance and oversight in the healthcare industry. The role requires expertise in governance, decision-making, and strategic planning to support organizational success in a Non-Executive Director capacity.