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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.
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。
The position of R&D Data & AI in Chemistry within the life sciences department requires expertise in data-driven methodologies and artificial intelligence applications. The role is based in Brentford and focuses on leveraging technology to enhance research and development processes in the business services industry.
Oversee product design and development for gummies and similar products to drive growth, focusing on China and other Asia regional markets.
This role is for a passionate Neuroscience Principal Scientist, who will contribute to the development of novel therapies for neurological disorders. The successful candidate will play a vital part in driving the company's innovative life science division in Shanghai.
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.
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。
生物首席科学家将负责生命科学领域的研究与开发,推动零售行业内的技术革新和产品优化。您将带领团队完成科学研究项目并支持公司的战略目标。
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 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.
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