Support the Manufacturing, Process Sciences (PS) and Quality Control (QC) departments through the troubleshooting, validation, transfer and application of analytical test procedures, and clinical product testing as needed Perform routine stability and release chemistry and biochemistry testing for pre-clinical and early clinical phase programs including techniques such as capillary electrophoresis (CE), ELISA, MCE, and iCIEFPerform assay qualification/validation experiments. Transfer new or improved control test procedures to customer groups. Troubleshoot established test methods used in development and release testing. Provide analytical support in troubleshooting process and formulation problems. Assist in the analysis of samples generated from lab scale process studies. Assist in product failure or customer complaint investigations Assist QC Release group with overflow routine testing Tabulate and report results quickly and accurately Present findings at group and possibly at interdepartmental meetings. Maintain lab supplies and equipment for GMP compliance. Produce and maintain accurate records. Train lower-level group members. 
