生命科学 jobs in China

This position focuses on managing regulatory affairs for FSMP (Food for Special Medical Purpose) products in China. The role ensures timely registration, compliance, and strategic regulatory planning without direct team management responsibilities.

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.

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.

统计负责人将在医疗保健行业中负责统计相关的核心工作，确保数据分析的准确性和可靠性。同时，您将为团队提供技术指导，推动项目成功实施。

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。

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。

临床检测负责人将负责监督和管理生命科学领域的临床检测项目，确保所有操作符合监管要求并达到高质量标准。该职位要求候选人具备深厚的专业知识和实际管理经验，以推动项目的高效执行。

该职位是一个重要的领导角色，专注于神经科学生物制剂的发现项目管理。候选人需具备专业的生命科学知识以及项目管理能力，推动项目的成功落地。

生命科学产业园项目，根据投资人要求，独立负责项目改造方案设计，后续对接施工单位进行深化落地。

作为一名PBI顾问，您将负责为生命科学行业内的会计和财务部门提供专业的业务智能解决方案。该职位需要熟悉数据分析工具和相关领域的专业知识，帮助提升决策效率。

作为一名P2P专家，您将在生命科学行业的会计与财务部门中负责处理端到端的采购到付款流程。此职位要求候选人具备扎实的财务知识和对流程优化的强烈兴趣。

该职位负责在数字部门中推动医药电商的广阔市场开发。候选人需要在生命科学行业中发挥创新和战略能力，以实现业务目标。

OTD总监负责为公司提供组织变革与发展支持，确保业务目标的高效实现。此职位需要在生命科学行业中具有卓越的战略视野和执行力。