GMP Document Control Coordinator -II
Listed on 2026-10-07
-
Quality Assurance - QA/QC
-
Administrative/Clerical
KBI Biopharma, Inc. is seeking a Document Control Coordinator I/II in Boulder, CO to manage cGMP-controlled documents throughout their lifecycle, including issuance, archival, retrieval, and destruction.
You will coordinate EDMS workflows, support internal and client audits and regulatory inspections, and serve as a liaison between QA, production, and customers to ensure timely documentation. This role requires strong attention to detail, organizational skills, and the ability to manage multiple
This role, GMP Document Control Coordinator I-II at KBI Biopharma, Inc., could be your next opportunity.
Join KBI Biopharma, Inc. and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the GMP Document Control Coordinator I-II role at KBI Biopharma, Inc., based in Boulder, CO, United States.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).