Night QA Manufacturing Specialist I/II — cGMP Batch
Listed on 2026-10-06
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Quality Assurance - QA/QC
Production QC/QA -
Manufacturing / Production
Production QC/QA
KBI Biopharma, Inc. seeks a Quality Assurance Specialist I/II Manufacturing to ensure products, processes, facilities, documentation, and systems meet quality standards, internal procedures, and regulatory requirements.
This role provides broad QA oversight for bulk drug substance manufacturing and reviews executed procedures, equipment logs, and batch records. The position involves authoring SOPs, supporting changeovers, resolving deviations, and collaborating across manufacturing, R&D, and QA
The Night QA Manufacturing Specialist I/II — cGMP Batch role at KBI Biopharma, Inc. is now open for applications in Boulder, CO, United States.
The advertised compensation is 67.000 - 85.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Night QA Manufacturing Specialist I/II — cGMP Batch role in the description above.
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