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The position involves performing functions associated with cGMP manufacturing operations within the biologics production facility. This includes working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components, and final materials. The role requires the use of sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments, or equipment. The individual will also determine and may assist in developing methods and procedures to control or modify the manufacturing process.
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