Life Sciences职位招聘信息

We are looking for an experienced CMO to lead the medical strategy and clinical development of our stem cell and regenerative medicine portfolio.

The role blends global technical leadership with local China accountability, acting as the single medical science point of contact for Greater China and the face of medical science to internal stakeholders, partners and external bodies.

The successful candidate will drive medical science-led innovation, evidence generation and commercial alignment, balancing scientific rigor, regulatory compliance and business growth across a diverse portfolio.

The Senior Director - Pipeline Strategy & Early Development will oversee the strategic planning and early development of innovative projects within the life sciences industry. Based in Beijing, this role requires a strong background in managing pipelines and driving early-stage development initiatives.

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.

The QC Assay Development Science Senior Director will oversee and manage quality control processes within the life sciences industry, ensuring compliance and efficiency. This role requires expertise in Assay Development sciences and a strong belief of quality standards in Shanghai

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.

This role is responsible for ensuring compliance with global export control regulations and customs requirements, while supporting business operations across China through risk management and regulatory guidance. The position also involves cross-functional collaboration, audit and licensing support, and driving process improvements to enhance trade compliance effectiveness and efficiency.

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。

数统总监将负责分析和管理生命科学领域的统计数据，为公司提供决策支持。该职位需要具备扎实的统计学知识和生命科学领域的专业背景。

担任整个国际化注册项目的负责人

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.