生命科学 jobs in Life Sciences

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.

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.

该职位负责制定和实施全球临床开发战略，确保产品开发符合行业标准和法规要求。候选人将与跨职能团队密切合作，推动生命科学领域的创新与发展。

临床医学SD-ED负责支持临床研究项目的设计、实施和管理，确保项目符合科学和法规要求。该职位适合对生命科学领域有深入了解并希望在临床研究中发挥重要作用的专业人士。

临床药理职位负责支持药物研发中的临床药理学研究工作，确保研究的科学性和合规性。该职位需要具有扎实的生命科学背景，并能够有效地与跨部门团队协作。

这是一份在商业服务行业中的质量控制（QC）职位，主要负责生命科学部门的质量管理和监督工作。该职位需要具备相关领域的专业知识，以及在香港工作的能力。

高级生物信息分析师将负责生命科学领域的数据分析和解读，支持业务服务行业的研究和开发。此职位要求候选人具备扎实的专业知识和分析能力，以提供高质量的解决方案。

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。

生物总监负责在生命科学领域推动业务发展，制定战略规划并领导团队实现目标。我们正在寻找一位具有专业知识和管理经验的候选人，能够在Brentford地区推动创新和成果。

药化总监将在零售行业的生命科学部门中，领导团队进行药物化学研发工作，推动项目从研发到实施的高效转化。此职位需要具备深厚的药物化学知识及项目管理能力，确保研究成果符合行业标准。

生物首席科学家将负责生命科学领域的研究与开发，推动零售行业内的技术革新和产品优化。您将带领团队完成科学研究项目并支持公司的战略目标。

The Drug Discovery Lead will be tasked with leading the development of operations in this exciting field and the development of a new drug discovery portfolio.