Life Sciences职位招聘信息

Join a rapidly expanding biotech as CSO, advanced scientific innovation from target identification through preclinical development while building a differentiated pipeline in oncology and immunology. We are looking for an industry-proven scientific executive with strong portfolio evaluation and drug discovery experience.

The Medical Director China will be responsible for incorporating and executing the local medical plan developed from the Global Medical and Marketing Strategical Plan incorporating local market and medical insights. This person will be accountable for Medical Governance and the medical ethical standards within the Country Organisation and takes full responsibility for the medical management in China - drives and leads all medical activities.

Provide scientific expertise in local registration clinical trials. and license-in OTC products.
Provide medical contributions in developing and implementing marketing strategy.

Translate complex scientific concepts into clear, credible brand narratives, strengthen collaborations with dermatology experts and scientific communities, and adapt global scientific storytelling for the Chinese market.

Oversee product design and development for gummies and similar products to drive growth, focusing on China and other Asia regional markets.

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.

负责支持蛋白纯化技术的转移与优化工作，确保技术转移过程的顺利进行。该职位要求在生命科学领域具备扎实的专业知识和实际操作能力。

将负责在生命科学领域支持技术转移和工艺优化，主要专注于微生物发酵技术的开发和实施。

我们正在为一家全球知名欧洲创新医药企业寻找一位 HR Shared Services Coordinator。

该岗位将加入亚太区HR Shared Services团队，负责员工全生命周期相关的人力资源运营支持，并作为员工与HR团队之间的重要桥梁，提供高效、专业的人力资源服务。

RNA药物成药性评估、递送体系理解以及IND申报经验

负责从靶点验证、药效评价、PD Biomarker开发到IND申报支持的全流程药理研究，兼顾团队指导与实验方案设计工作。

负责搭建和领导多肽药物分析研发平台，统筹分析方法开发、技术转移、注册申报及商业化支持等全生命周期分析工作。带领高水平团队解决复杂多肽药物分析技术挑战，推动创新项目高质量交付并支撑公司全球化发展。

The Global Director, Quality Assurance & Regulatory Affairs will lead the company's global QARA function, overseeing quality systems, regulatory compliance, audits, supplier quality, and market access activities across international markets. This role will manage a team of QA and RA professionals while collaborating with cross-functional stakeholders, external regulatory bodies, notified bodies, distributors, and regional regulatory partners worldwide.

The Regulatory Affairs Manager will lead regulatory activities in China, ensuring product compliance, registration execution, and effective engagement with regulatory authorities and external partners.

This role serves as a key business partner to commercial, quality, innovation, supply chain, and global regulatory teams, supporting market access and long-term portfolio growth.

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.

小核酸事业部负责人将在杭州领导生命科学领域的核心业务发展，推动团队实现战略目标并在行业内取得更大突破。此职位要求具备丰富的管理经验和对小核酸技术的深刻理解。

负责蛋白表达平台的生产运营与团队管理，统筹外部客户订单交付，持续优化生产工艺，保障质量、产能及交付效率。

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.