Sterile Equipment Validation Lead
Listed on 2026-10-12
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Healthcare
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Pharmaceutical
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
We are looking to fill the Sterile Equipment Validation Lead position at Hikma Pharmaceuticals in Bedford, OH, United States.
This role, Sterile Equipment Validation Lead at Hikma Pharmaceuticals, could be your next move.
Are you ready to take on the Sterile Equipment Validation Lead role at Hikma Pharmaceuticals?
We would love to welcome a new Sterile Equipment Validation Lead to our organisation in Bedford, OH, United States.
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