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strategically set up a new business line of life science parks from 0 to 1
You will lead translational research and early clinical development strategies, bridging discovery science with clinical application. The position combines scientific leadership, operational oversight, and regulatory engagement to accelerate innovative therapies toward commercialization.
The VP of Corporate Strategic Investment is responsible for identifying, executing, and integrating inorganic growth, revenue-generating technology platform M&A deals that accelerate the company's commercial and operational capabilities.
In partnership with the CEO, the position holder will lead the company's science and research strategy and implementation. The person will take leadership role in shaping the scientific strategy and bringing new product into the company to build strong product pipeline. He/she will identify potential leads, formulate transaction model, lead business negotiation, and manage the execution of the transactions
In partnership with the CEO, the position holder will lead the company's business development strategy and implementation. The person will take leadership role in shaping the portfolio strategy with focus on out-licensing and partnership opportunities. The candidate will identify potential leads, formulate transaction model, lead business negotiation, and manage the execution of the transactions.
The Senior Sales Manager will be accountable for global sales for genomic sequencing and proteomics services. This role combines hands-on sales management, business development, growing a sales team, developing commercial strategy and delivering a straightforward, competitive offering to global clients.
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.
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.
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.
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