Sterile Equipment Validation Lead

Hikma Pharmaceuticals · Bedford, United States

Hikma Pharmaceuticals USA Inc. in Bedford, OH seeks an Equipment Validation Supervisor to lead qualification programs for sterile and injectable manufacturing.

You will manage a team, oversee IQ/OQ/PQ, and ensure compliance with FDA, EU GMP, and global standards while driving CAPA and continuous improvement. You will collaborate with Engineering, Manufacturing, QA, and Regulatory Affairs on new product introductions, capacity expansion, and risk-based validation strategies, with a focus on