Performs analyses, including, but not limited to, biochemical and/or chemical analyses of raw materials, in lab bench testing of raw materials, appearance, FTIR, Identity testing, UV, Karl-Fisher titrations, Acid-Base titrations, HPLC, LC-MS, GC, GC-MS, NMR, ICP-M. Knowledge of cGMP guidelines as well as international regulations (i.e., International Committee on Harmonization (ICH) Q7) pertaining to Quality Control programs that support production of APIs, stability and drug product release.