CGMP Quality Assurance Associate: Documentation
Job in
Maple Grove, Hennepin County, Minnesota, 55311, USA
Listed on 2026-08-12
Listing for:
Bora Pharmaceuticals
Full Time
position Listed on 2026-08-12
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Production QC/QA
Job Description & How to Apply Below
Bora Pharmaceuticals is seeking a Quality Associate to support cGMP documentation, batch review, and final disposition in manufacturing and packaging operations. This role emphasizes rigorous documentation and adherence to quality procedures within FDA-regulated processes.
The position also involves investigations, document lifecycle administration, and collaboration with Operations to ensure compliance. ASQ CQI/CQA certification is a plus for the candidate pool.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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