About this opportunity
Hikma Pharmaceuticals lists this Sterile Equipment Validation Lead opportunity in bedford, Ohio. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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
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Worksite address
bedford, OH, 44146, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.