Stability Programs Coordinator

Hikma Pharmaceuticals USA Inc. in Bedford, Ohio, seeks a Stability Administrator to coordinate stability programs for oral and sterile products.
You will manage sample lifecycles, ensure data integrity, and prepare stability reports for regulatory submissions in a regulated manufacturing environment. The role requires 2–5+ years in stability/QC/GMP within FDA-regulated settings, with a Bachelor's degree in a related field and knowledge of ICH guidelines.

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