This job was posted by https://illinoisjoblink.illinois.gov : For more information, please see: https://illinoisjoblink.illinois.gov/ada/r/jobs/7395241 Contribute to the in-process and release testing of pharmaceutical finished products produced on site. Contribute to the Quality Control (QC) Chemist and Microbiologist functions and responsibilities. Participate in the operation and maintenance of the polarograph and gamma spectrometer. Perform required analytical testing on in-process and final products. Perform required bioburden, sterility and bacterial endotoxin testing on final products and raw materials. Perform viable and non-viable environmental monitoring. Operate non-viable particle counter/facility monitoring systems. Execute and maintain stability programs. Serve as the attending Microbiologist during aseptic manufacturing; perform auditing and environmental monitoring during production. Perform investigations of OOS results and implement CAPA plans and change controls. Conduct training of QC chemists. Understand the acceptance activity requirements for incoming, in-process and final inspection requirements to ensure the product conforms to its specification and out-of-specification items are properly handled. Understand the stop orders, concessions, CAPA, calibration, preventative maintenance, material identification & segregation, documentation configuration control practices; documentation & disposition of non-conforming material, Good Documentation Practices requirements and Part 11 compliance. Comply to the Quality Manual, Quality Management System, Quality Management Policy, Quality Goals and applicable laws and regulations. Identify and report any quality or compliance concerns and take immediate corrective action, as required.