Yijun Cheng
About Yijun Cheng
Yijun Cheng is the Associate Director Of ARD at BeiGene in Suzhou, China, with extensive experience in the medical device industry and expertise in LC-MS and GLP.
Current Role at BeiGene
Yijun Cheng is currently serving as the Associate Director Of Analytical Research and Development (ARD) at BeiGene. Based in Suzhou, Jiangsu, China, Cheng has been in this role since March 2021. In this capacity, she is likely involved in managing and guiding research and development projects relating to the analysis of pharmaceutical products. Her work may include the development and validation of analytical methods, ensuring compliance with regulatory standards, and contributing to the overall research and development strategy of the company.
Previous Positions
Before her current role, Yijun Cheng held the position of Sr. Manager in the CMC ARD department at BeiGene from 2019 to 2021. She also has extensive industry experience from her six-year tenure at Baxter International Inc., where she served as Manager I from 2013 to 2019 in Suzhou, Jiangsu, China. These roles would have provided her with significant expertise in managing complex research projects, developing pharmaceutical products, and navigating regulatory requirements.
Educational Background
Yijun Cheng obtained her Doctor of Philosophy (PhD) in Pharmaceutical Engineering from East China University of Science and Technology. She studied there from 2002 to 2011. During her doctoral studies, she would have gained in-depth knowledge and technical skills relevant to pharmaceutical sciences, which laid the foundation for her career in the life sciences and medical device industry.
Expertise in Laboratory Techniques and Regulations
Yijun Cheng has specialized expertise in Liquid Chromatography-Mass Spectrometry (LC-MS) and Good Laboratory Practice (GLP). She is also experienced in validation processes within the medical device industry and is familiar with U.S. Food and Drug Administration (FDA) regulations. Cheng's proficiency in these areas supports her role in ensuring that analytical methods and processes meet stringent regulatory and quality standards.
Experience in the Medical Device Industry
Yijun Cheng has a demonstrated history of working in the medical device industry. Her background includes significant work related to the validation of medical devices and adherence to regulatory standards set by bodies such as the FDA. This experience is crucial for ensuring that medical devices are developed and tested in compliance with regulatory and safety standards.