TRANSCENTA HOLDING - A Global Fully Integrated Biotherapeutics Company
Transcenta, Biologics, Antibody, Claudin 18.2
1. Responsible for the formulation screening, stability study and clinical compatibility study. Perform experiments in strict accordance with the operating procedures, conduct physical- chemical test, analysis and represent data, write the technical report so on.
2. Lead the formulation development work of specific project to meet the IND/BLA filing timeline. Capable to solve the problems on the basis of science and optimize the formulation and process to better deliver target.
3. Have an extensive and in-depth understanding of relevant bio-pharmaceutical knowledge, such as protein degradation, stress factor and particle control. Master in the key technique such as DSC, DLS and viscosity analysis.
4.Understand the basic requirements of pharmacopeia and official guideline about drug development research and filing.
1.Identify the corporate culture of the company and be enterprising and responsible for the job
2.Undergraduate 5 ~10 years or master's degree3 ~ 7 years of work experience;
3.Have a background in pharmaceutics, pharmacy, chemistry, bioengineering or biotechnology and other related professional education, and have experience in antibody and formulation development is preferred;
4.Be rigorous, diligent, studious, hard-working, team spirit, have a certain ability to work under pressure;
5.Have a certain ability of English Reading.