CGMP Quality Assurance Associate: Documentation
Bora Pharmaceuticals
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-Ljbffr Bora Pharmaceuticals
Vacancy posted 3 days ago
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