Ruiting Liang
About Ruiting Liang
Ruiting Liang is the Director of Analytical R&D at BeiGene in Beijing, China, with extensive experience in multi-modality pharmaceutical development and global regulatory compliance.
Current Role at BeiGene
Ruiting Liang is currently the Director of Analytical Research and Development (R&D) at BeiGene, based in Beijing, China. In this role, Liang is responsible for overseeing the analytical aspects of pharmaceutical development, ensuring that both internal and external projects meet the company's rigorous standards. Liang's extensive background in pharmaceutical R&D positions them as a pivotal figure in driving BeiGene's innovation and development strategies.
Previous Experience at Amgen
Before joining BeiGene, Ruiting Liang worked at Amgen as a Senior Scientist in Process Development from 2019 to 2021. Based in Cambridge, Massachusetts, Liang's role involved significant contribution to process improvement and development in the pharmaceutical sector. This experience further honed Liang's skills in developing end-to-end control strategies and managing comprehensive research projects.
Earlier Roles in Analytical R&D
Ruiting Liang has a broad spectrum of experience in Analytical R&D, having worked at several prominent organizations. This includes a stint at Alkermes as a Senior Scientist, Analytical R&D, for eight months and at Biogen as Scientist II, Technical Development, for three years. Liang also spent five years at Nitto Avecia as an Analytics Development Chemist II. These roles have collectively fortified Liang's expertise in multi-modality pharmaceutical development, encompassing nucleic acids, small molecules, and biologics.
Academic Background
Ruiting Liang holds a Doctorate in Chemistry and Biophysical Chemistry from the University of Rochester, which they earned after seven years of rigorous study. Prior to this, Liang received an Associate in Computer Software Engineering and a Bachelor's in Chemistry from Peking University. This blend of diverse educational qualifications underpins Liang's multidisciplinary approach to pharmaceutical R&D.
Skills and Expertise
With over a decade of experience in the pharmaceutical industry, Ruiting Liang possesses a robust portfolio of skills. Liang is proficient in CMC project management, has a solid grasp of global regulations including FDA, EMA, MHRA, and ICH guidelines, and is experienced in global regulatory filings and RTQs. Liang has developed and executed outsourcing strategies effectively, managing external suppliers to meet development timelines. Demonstrating strong managerial skills, Liang excels as a people manager and cross-functional leader, promoting collaboration, innovation, and efficient decision-making.