Purpose Statement

• Performs functions associated with cGMP manufacturing operations within the biologics production facility.
• Completes batch documentation accurately and thoroughly, while adhering to the required quality and safety standards, and in a productive, cost-effective manner.
• Serves as a highly skilled subject matter expert within the manufacturing area, contributing to the development of concepts, techniques, and process improvements.
• Supports and drives troubleshooting efforts during course of shift work to ensure adherence to schedule and production plan. 

Major Responsibilities:

• To perform purification operations that include column chromatography, tangential flow filtration, Viral filtration and Bulk filling in Glovebox within the biologics production facility
• Execute on computerized systems (suc...