Associate Director-Regulatory Affairs - Beijing

We are seeking a Regulatory Affairs Director to join our team at B. Braun in Beijing. · Bachelor's degree or above in a science and engineering-related major. · Total working years >= 15 years in medical industry with 5 years above management experience on large team size (10+ em ...

+ Job summary: The Regulatory Affairs Director is a key leadership role responsible for driving the end-to-end regulatory strategy and execution for Gilead's portfolio in China, with a primary focus on oncology and inflammation therapeutic areas.+ Bachelor's degree or higher in P ...

Join us in at B. Braun, a leader in the medical devices industry, where your skills and experience will be recognized and celebrated. · ...

Join us in at B. Braun, a leader in the medical devices industry, where your skills and experience will be recognized and celebrated.Take the next step in your career with us and help shape the future of healthcare · ...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve th ...

Lead regulatory affairs projects in China to ensure timely approval and compliance; support strategic initiatives from regulatory perspective. · ...

Lead the planning and implementation of assigned product registration projects in China to ensure timely approval and regulatory compliance. · ...

Directly report to Head of Global Regulatory Affairs (ex-China), represent GRA ex-China to lead the project management & strategic inputs on assigned products/projects. · ...

Applying, · obtaining and maintaining regulatory approvals for products within Amgen's portfolio. · ...

Working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. · ...

Career Category · Regulatory · Job Description · Regulatory Affairs Manager- China · Reporting to: Head of Regulatory Strategy, China RA · Based in: Beijing · Job Description · Applying, obtaining and maintaining regulatory approvals for products within Amgen's portfolio, includi ...

We need your talent, knowledge and dedication to better our world with biology. · In Novonesis, we know that solutions rooted in biology can help solve humanity's biggest challenges. · ...

This is work that transforms the lives of patients and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope alongside high-achieving teams. · We are seeking Regulatory Affairs Specialist to support our regulato ...

We are looking for a Regulatory Affairs Specialist who will unite caring with discovery to make life better for people around the world. · ...

This position is responsible for assisting RA department, include but not limit to getting market clearance for Getinge products, · contacting factories and NMPA, · and other RA operation related work.Prepare the documents for NMPA review: Request the registration documents from ...

We are seeking a Regulatory Affairs Principal to assist our RA department in various tasks including market clearance for Getinge products, contacting factories and NMPA, and other RA operation related work. As a key member of our team you will prepare documents for NMPA review, ...

This position is responsible for assisting RA department, include but not limit to getting market clearance for Getinge products · 该职位负责协助RA部门,包括但不限于根据RA Leader的安排支持洁定产品注册获取市场准入许可 · Prepare the documents for NMPA review: Request the registration documents from factory side; Prepa ...

We need your talent, knowledge and dedication to better our world with biology. In this role you will be responsible for registration work of new GMM feed additives and microbes in China. · Ensure market access for animal health products in China by preparing submission, registra ...

Manages regulatory strategy and operations for assigned regions. · ...

Directs the development of submission of product registration, progress reports, supplements, amendments and/or periodic experience reports. Provides strategic product direction to teams on interaction and negotiates evidence with regulatory agencies. · Serves as a regulatory lia ...