Hikma Pharmaceuticals USA Inc. in Bedford, Ohio is seeking a Stability Administrator to coordinate stability programs for oral and sterile products.
You will maintain schedules, manage samples, and ensure data integrity in cGMP-compliant systems, while supporting regulatory submissions and audits. The role requires 2–5+ years in stability/QC in FDA-regulated environments, with preference for injectable or sterile product experience.
#J-18808-LjbffrStability Program Lead in northern at Unknown Company
This position is listed as full time and onsite.