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