Quality Assurance Associate - cGMP & Documentation
Bora Pharmaceuticals Inc
Bora Bora Pharmaceuticals is seeking a Quality Associate to support cGMP documentation, batch record review, and QA approvals in a regulated manufacturing environment. You will handle document lifecycle and assist with investigations under QA Management. Experience in FDA-regulated settings is required. Preferred ASQ certification, strong attention to detail, and ability to work with operations to drive compliance and quality improvements. #J-18808-Ljbffr Bora Pharmaceuticals Inc
Vacancy posted 4 days ago
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