- Amgen (Washington, DC)
- …Basic understanding cGMP requirements + Experience related to upstream and/or downstream biologics process development technology transfer, scale-up and ... process improvements + Work with research, manufacturing, maintenance, process development , utilities, facilities, quality assurance and/or validation… more
- Catalent Pharma Solutions (Harmans, MD)
- …I/II bulk biologics Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and ... biopharmaceutical manufacturing/R&D facility, supporting the GMP production of Phase I/II bulk Biologics + Must obtain Grade 3 Stationary Engineer 's License… more