生命科学职位招聘信息

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。

Lead regulatory affairs activities for Thailand operations and support market access, product compliance, and registration activities across key ASEAN markets.

Serve as the regional regulatory expert, providing strategic guidance on formulations, ingredients, claims, labeling, and regulatory pathways for both local and export markets.

从零搭建完整医学事务体系，覆盖上市前研究、上市后支持及医学传播全链路。

以业务结果为导向，构建"证据+专家+传播"的医学能力，直接参与商业落地。

This role oversees end-to-end regulatory affairs for the China business: market entry, standards and labeling, claims and packaging compliance, risk identification and response, and professional engagement with authorities and industry bodies. It requires managing multiple projects in a fast-paced, results-oriented environment and partnering with R&D, FSQ, Marketing, Legal and Supply Chain to secure compliance across the product lifecycle.

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 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.

作为一名首席科学家，您将负责主导生命科学领域的研究与开发项目，推动创新技术的应用，并为团队提供技术指导和战略支持。

As a key member of the executive management team (CEO/General Manager), you will take full responsibility for overall business operations and lead the company through the critical transition from product registration to launch and commercial execution.

- 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

作为公司战略运营核心负责人，统筹战略制定、执行监控及跨部门协同，推动战略转化为经营成果。

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.

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。

财务总监职位设于上海，主要负责生命科学行业的人力资源部门的财务管理工作，确保财务运营的高效和合规。

• 负责生命科学/医疗业务的法律与合规支持，重点涵盖研发、临床数据合规及中美监管要求，并制定相关合规政策及培训。
• 负责商业合同及公司事务法律支持，包括研发合作、临床试验、许可转让、CRO/CDMO等协议，以及ESOP、融资等项目。