CGMP Manufacturing Coordinator
Listed on 2026-10-18
-
Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing & Industrial Operations, Production Associate / Production Line, Production QC/QA
STERIS is seeking a Manufacturing Coordinator to support aseptic operations by coordinating production documentation, lot control, and inventory reconciliation. This role collaborates with Manufacturing, Quality, and Supply Chain to ensure compliant documentation and timely product release.
The position emphasizes accurate record-keeping, adherence to cGMP, and continuous process improvement while minimizing production delays. Daytime hours with potential overtime in a regulated environment.
Step into the cGMP Manufacturing Coordinator role at STERIS
- Operations in St. Louis, MO, United States and grow with us.
We are currently recruiting a cGMP Manufacturing Coordinator for our team in St. Louis, MO, United States.
This is a strong role to take on the cGMP Manufacturing Coordinator role at STERIS
- Operations.
As a cGMP Manufacturing Coordinator, you will play an important part at STERIS
- Operations in St. Louis, MO, United States.
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