全国职位 - 生命科学类别

As the 'Head of China Development' you will be appointed to oversee the strategic and operational agenda in the field of vaccines for all China domestic related development activities, manage a cross functional team of representatives from all development functions and chair the China Development Management Team (CDMT) to advance new targets and candidate products.

Page Executive is seeking experienced industry Executive interested to join early growth biotech investment fund. You will take responsibility to establish post-investment strategy and process to support long-term growth for portfolio of invested and incubated companies.

Prefer candidates with 2-3 year experiences in regulatory affairs.

A great opportunity for candidates with management consulting background to make a career progress.

从市场引进技术或高校科研机构可转化的成果进行评估及转化实施

将核酸化学应用于RNA编辑或RNAi药物分子设计

• 全面负责纳米制剂的工艺技术开发及工艺优化研究，解决项目研发过程中的关键技术问题，把控研发节点，评估项目进展，降低产品风险；

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.

1. 进行中国医疗器械产品注册、临床的咨询和协调工作；

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.

Page Executive is seeking experience Head of Research and Developement Science to oversee innovation pipeline development for domestic pharmaceutical company with focus on metabolic and chronic disease management.

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.

结合药厂业务战略规划，编制年度预算及工作计划，设计内部流程、职能划分及绩效方案，监督和管理实验室的日常运作，确保所有实验遵循适用的法规、指南及公司SOP 标准执行

The Enzyme R&D Director will oversee enzyme discovery, production technology, purification, and process scale-up to ensure the delivery of high-quality enzyme products that meet the company's strategic goals.

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.

1. 该岗位需领导多职能研发团队，负责咸味零食研发战略规划、项目开展及与各部门合作等工作。
2. 要求具备相关专业学历、丰富经验、团队管理能力及对各领域的深入了解和创新能力。

制剂学术带头人（吸入/透皮/高端制剂方向）

* Lead the new open development cosmetics and personal care medical device products in China.
* Identify trendy texture and work on the pre-development of formula for push opportunities.

The China Regulatory Affairs Manager will provide leadership and strategic direction for the Regulatory department in China.
They will ensure that all local regulatory requirements are met throughout product lifecyle, from guiding formula development and innovation, to reviewing marketing/advertising materials such as labels and securing advertising permits, to handling post-launch reporting.

负责对于新型多肽分子的设计、合成和纯化，并评估其体外/体内药效特性等