生命科学 jobs in China

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.

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.

肿瘤领域CMO负责推动肿瘤领域项目的临床开发和实施，确保项目符合行业标准并取得成功。您将与研发团队紧密合作，制定战略并监督执行，以推动关键项目的进展。

中成药医学负责人将负责公司中成药产品的医学策略制定和实施，确保相关产品符合行业标准并支持市场需求。该职位要求候选人具备扎实的中医药知识及医学专业背景，能够推动产品的医学价值。

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。

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。

高级生物信息分析师将负责生命科学领域的数据分析和解读，支持业务服务行业的研究和开发。此职位要求候选人具备扎实的专业知识和分析能力，以提供高质量的解决方案。

抗体研发项目总监负责生命科学领域的研发项目管理，确保项目按时、高质量完成。此职位需要具备丰富的专业知识，并能够高效协调团队资源，推动项目成功实施。

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。

作为医疗经理，您将负责在快速消费品行业中支持与生命科学相关的项目管理和执行，为公司业务目标的实现提供专业的医学支持。该职位要求候选人具备医学领域的专业知识，并能在北京地区高效开展工作。

器械营销总监负责制定和实施销售战略，推动公司在生命科学领域的市场份额增长。此岗位需要具备卓越的销售管理能力以及对生命科学行业的深入了解。

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。

财务副总裁将负责全面管理公司财务运营，确保财务策略与公司在生命科学领域的整体目标一致，该职位需要具备卓越的财务分析能力和战略规划能力。