Description: The Quality Control Analyst is responsible for conducting the cell-based potency assays(CBPA) of biologics for release and stability of both commercial and late-stage biologics under current good manufacture practice(cGMP). ...
and biological drugs (e.g manufacturing and QC of clinical trial material, stability testing, test method transfer). Strong working... during clinical development of pharmaceutical and biological drugs (e.g manufacturing and QC of clinical trial material, stability...