浏览我们的职位并开启您的下一步申请
只需点击几下,即可找到合适的候选人。
PageGroup通过创造挖掘潜能,让您绽放自我,成就精彩人生
如果您有任何问题,我们很乐意为您提供帮助。
The RA Director position in the life sciences industry requires expertise in regulatory affairs to oversee compliance and ensure successful product approvals. Based in Beijing, this role is integral in driving regulatory strategies and supporting product life cycles.
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 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.
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
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 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.
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.
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.
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.
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.
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.
Create Job alert to receive 总裁 生命科学 jobs via email the minute they become available
Submit your CV to register with us and we will contact you if a suitable role becomes available.