Night QA Manufacturing Specialist I/II — cGMP Batch
-
Quality Assurance - QA/QC
-
Manufacturing / Production
Job Description & How to Apply Below
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
This is a strong role to take on the Night QA Manufacturing Specialist I/II — cGMP Batch role at KBI Biopharma, Inc.
We have an opening for a Night QA Manufacturing Specialist I/II — cGMP Batch in Boulder, CO, United States within Engineering.
This role, Night QA Manufacturing Specialist I/II — cGMP Batch at KBI Biopharma, Inc., could be your next move.
Are you ready to take on the Night QA Manufacturing Specialist I/II — cGMP Batch role at KBI Biopharma, Inc.?
(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).
View / Apply for Jobs
Matching My Jurisdiction