Performs functions associated with cGMP manufacturing operations within a biologics production facility. The role includes working with engineers on setup and calibration tasks, and performing rework and quality testing related to production of parts, components, and final materials. Uses programs such as LIMS, SAP, and automated control systems to collect and evaluate operating data, which may be used to make on-line adjustments to products, instruments, or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process. The position follows the UD Fill A1 shift: 7:00 a.m.–7:30 p.m. Sunday, Monday, and Tuesday, and every other Wednesday.
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Job Type
Full-time
Career Level
Senior