Life Sciences职位招聘信息

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 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.

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。

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.

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。

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.

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。

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.

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。

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.

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。

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。

这是一份位于上海的全职职位，主要负责上市前医学相关的管理与支持工作。我们正在寻找一位有能力推动生命科学行业发展的专业人士加入我们的团队。

- 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

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。