To perform QC analytical testing in support of biologics bulk drug substance manufacturing using defined methods in a cGMP compliant laboratory. Assures test results are accurately recorded and abnormal data or equipment/instrument malfunctions are promptly reported to his/her supervisor
Performs routine testing and data review of batch release and stability samples of Bulk Drug Substance in a cGMP compliant environment.
Performs routine assays such as UV-VIS Spectrometry, SDS Page and various HPLC methodologies, (e.g. SEC and reverse phase).