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The Medical Advisor will play a crucial role in providing medical and scientific expertise within the life sciences industry. Based in Beijing, this position involves supporting medical strategies and ensuring compliance with medical guidelines and regulations.
The Medical Advisor role in the Life Science industry requires a professional with expertise in medical strategy and scientific communication.
We are looking for an experienced CMO to lead the medical strategy and clinical development of our stem cell and regenerative medicine portfolio.
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.
Oversee product design and development for gummies and similar products to drive growth, focusing on China and other Asia regional markets.
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.
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.
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.
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.
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。
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.
Lead the development and validation of nutrition-related claims by transforming scientific evidence into consumer-relevant messaging aligned with business strategy.Partner closely with marketing, regulatory, and R&D teams to ensure all communication is scientifically sound and compliant with local requirements.
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.
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.
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 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.
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.
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.
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