Quality Control Senior Associate - (Chicago, IL)

Summary: 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 Responsibilities: * Performs routine testing and data review of raw materials samples and, in-process, batch release and stability samples of Bulk Drug Substance in a cGMP compliant environment. * Performs routine assays such as UV-VIS Spectrometry, SDS Page, Wet chemical analysis, various HPLC methodologies (e.g. SEC and reverse phase), utility testing (e.g. TOC, conductivity, and gas testing.) * Performs sample management including: sample receipt, sample tracking, aliquots preparation, and sample distribution * Writes and revises SOPs for managerial review and approval. * Aids in troubleshooting equipment and methods and performs some basic troubleshooting techniques.