• Perform batch record review for a range of preparation, formulation, and filling lines across multiple buildings.• Regularly attend meetings to present and evaluate potential deviations, prevention methods, and process improvement methods.• Utilize programs such as Trackwise, JDE, LIMS, and MES for deviation initiation/writing, tracking labor hours, SOP writing/revision, and sample tracking.• Assist in the implementation and evaluation of FDA CAPAs

• Assisted in leading a manufacturing team of 15 to 20 employees• Operated a range of automated packaging/inspection equipment• Regularly trained coworkers on equipment, as well as other processes• Acted as a resource for colleagues

• Operated a range of automated packaging equipment