1. Review lab data. Including daily and periodic review work. 2. Perform instrument qualification and analytical method validation/verification. 3.Establish and revise SOPs and test procedures according to regulations/SOPs and Pharmacopoeia or registration specification. 4. Provide technical support to other department.
WHO YOU ARE 1. Education: Bachelor degree or above in pharmaceutical analysis or related major. 2. Experience: 5 years of working experience in quality control in pharmaceutical industry. 3. Have the ability to identify potential risks and deal with risks in time. 4. Have fluent English in reading, speaking and writing. 5. Familiar with Ch.P/USP/EP and lab related GMP documents, especially data integrity topic 6. Be familiar with the operation of instruments in QC Lab, e.g.: HPLC, GC, AAS, UV. 7.Have good team cooperation spirit.