ASAT Chemist Manager is responsible for providing technical analysis expertise, conducting analytical technology transfer projects, and supporting laboratory troubleshooting and continuous improvement. The role also involves supporting ongoing product development and registration, participating in the creation and revision of standard operating procedures, and evaluating and implementing new technologies.
Requirements
- Bachelor's degree or above (985 and 211 universities are preferred), related majors such as biochemistry, bioanalysis, analytical chemistry
- More than 7 years of relevant work experience in GMP biopharmaceutical companies
- Rich experience in analysis and quality control in the pharmaceutical industry; experience with HPLC and CE method validation
- Familiarity with global pharmaceutical regulations related to bioquality control (ICH, NMPA, FDA, EMA, USP, ChP, EP) and a certain understanding of GMP requirements
- Familiarity with bioquality control-related instruments, method development, and method validation
- Strong independent thinking and analytical ability, able to propose solutions based on actual situations
- Strong personnel management ability, project management ability, and good communication skills
- Good team spirit, responsible work, and considerate thinking
- Good English listening, speaking, reading, and writing ability