全国职位 - 生命科学类别

This role is responsible for developing and implementing China-focused early clinical development strategies to generate high-quality, decision-driving data for global programs across genetic neurological, renal, pulmonary, and other rare genetic diseases.

知名MNC平台专注CTA方向发展，深度参与创新药从研发到临床转化的关键节点。岗位为1年contractor形式开始，长期续签

An exciting National Medical leadership opportunity for an experienced Medical Affairs professional to drive scientific exchange and stakeholder engagement across China. The role offers significant autonomy, exposure to senior leadership, and the chance to contribute to the future growth of the Medical Affairs organization.

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.

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.

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。

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。

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.

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 Sr. Research Scientist is responsible for driving scientific research and substantiation, including literature review, in-vitro, preclinical and clinical studies, to support product development and innovation.

The role also provides scientific communication support to marketing and sales teams, translating research outcomes into evidence-based product claims, training content, and external presentations.

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.

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.

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.

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.

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。