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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.
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。
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.
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。
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.
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.
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.
战略并购副总裁将在生命科学领域中,负责推动并购项目的战略规划与执行,确保项目的成功落地。该职位需要强大的财务分析能力和并购经验。
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 China BD Director role is a fantastic opportunity for a seasoned professional with expertise in business development within the life science industry. Based in Pensacola, this position focuses on driving growth and fostering partnerships in the Chinese market.
The Supplier Quality Manager in Shenzhen will oversee and enhance supplier quality processes within the life science sector, ensuring compliance with industry standards. This role requires expertise in engineering and manufacturing to maintain and improve supplier performance.
The role of China BD Head in the life science industry is an exciting opportunity to lead business development efforts, drive strategic partnerships, and foster growth in the Shanghai region. The position requires a results-oriented professional with a strong understanding of the life science sector and a proven ability to identify and secure new opportunities.
This Data Operation role in the Life Science industry offers an excellent opportunity to support and manage data processes within the Technology department.
This is an exciting opportunity for an experienced professional to lead AI transformation initiatives within the life science industry. Based in Shanghai - Pudong, the role involves driving technological advancements to enhance operational efficiency and innovation.
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