Night QA Manufacturing Specialist I/II cGMP & BatchRecords
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Quality Assurance - QA/QC
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Manufacturing / Production
Job Description & How to Apply Below
KBI Biopharma is seeking a Quality Assurance Specialist I/II Manufacturing to ensure products, processes, facilities, documentation, and systems meet quality standards and government regulations. This role provides broad QA oversight for activities supporting bulk drug substance manufacturing.
Responsibilities include review and approval of batch records, SOPs, deviation investigations, and collaboration with GMP teams to resolve deviations promptly. Night shift with shift differential.
Our group is growing, and we are hiring a Night QA Manufacturing Specialist I/II cGMP & Batch Records in Boulder, CO, United States.
This opportunity is for the Night QA Manufacturing Specialist I/II cGMP & Batch Records role at KBI Biopharma.
We are seeking a motivated Night QA Manufacturing Specialist I/II cGMP & Batch Records to join KBI Biopharma in Boulder, CO, United States.
Consider building your career as a Night QA Manufacturing Specialist I/II cGMP & Batch Records at KBI Biopharma.
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