Quality Assurance Associate — cGMP Documentation
Job in
Maple Grove, Hennepin County, Minnesota, 55311, USA
Listed on 2026-08-11
Listing for:
Bora Pharmaceuticals
Full Time
position Listed on 2026-08-11
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist, Pharmaceutical Manufacturing
Job Description & How to Apply Below
Bora Pharmaceuticals is a premier CDMO focused on formulation development, clinical and commercial manufacturing, and packaging. The Quality Associate issues cGMP documentation to operations, reviews batch records, and performs final disposition to ensure compliant manufacturing and packaging processes.
Ideal candidates have a strong attention to detail, experience in FDA-regulated environments, and proficiency in documentation control.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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