KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force.
The Document Control Coordinator I / II is responsible for reviewing, controlling, and issuing cGMP documentation in support of regulated manufacturing and quality operations. The role ensures documentation accuracy, compliance with cGMP requirements, and adherence to internal documentation standards and procedures.
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force.
Integrated Resources, Inc ( IRI )