GMP Document Control Coordinator I/II - Lifecycle & Audits
Listed on 2026-10-30
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Quality Assurance - QA/QC
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Administrative/Clerical
KBI Biopharma, Inc. is seeking a detail‑oriented Document Control Coordinator I/II to manage GMP‑controlled documents throughout their lifecycle, support audits, and ensure accurate records for internal teams and clients.
The role emphasizes timely issuance, review, archival, and retrieval to uphold data integrity and regulatory compliance. You will coordinate cross‑functional document workflows, maintain EDMS and paper files, respond to documentation requests, and assist with inspections and
Consider building your career as a GMP Document Control Coordinator I/II
- Lifecycle & Audits at KBI Biopharma, Inc.
We are currently recruiting a GMP Document Control Coordinator I/II
- Lifecycle & Audits for our team in CO, United States.
This is a strong opportunity to take on the GMP Document Control Coordinator I/II
- Lifecycle & Audits role at KBI Biopharma, Inc.
As a GMP Document Control Coordinator I/II
- Lifecycle & Audits, you will play an important part at KBI Biopharma, Inc. in CO, United States.
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