Stability Program Lead — FDA-Regulated Pharma
Hikma Pharmaceuticals
Hikma Pharmaceuticals USA Inc. is seeking a Stability Administrator to coordinate stability programs for oral and sterile injectable products, ensuring compliance with ICH, FDA, and cGMP requirements. You will manage sample lifecycle, data integrity, and inspection readiness in regulated manufacturing environments. The role involves cross-functional collaboration with QC, QA, Regulatory Affairs, and Manufacturing to support stability studies, regulatory submissions, and lifecycle management, #J-18808-Ljbffr Hikma Pharmaceuticals
Vacancy posted 15 hours ago
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