Purpose: 

• Performs functions associated with cGMP manufacturing operations within the biologics production facility, including 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.
• Completes batch documentation accurately and thoroughly, while adhering to the required quality and safety standards, and in a productive, cost-effective manner.
• Supports operations & troubleshooting efforts during course of shift work to ensure adherence to schedule and production plan.

Major Responsibilities:



Key Responsibilities Summary:

• Performs cGMP upstream manufacturing operations (e.g., vial thaw, inoculation, cell culture, and recovery).
• Works with engineers on setup and calibration tasks, as well as performing rework and quality testing re...