Summary from listing
Hikma Pharmaceuticals USA Inc. is hiring a full-time Equipment Validation Supervisor in Bedford, Ohio, to lead equipment qualification and validation activities across manufacturing and laboratory systems, with emphasis on sterile and injectable product environments. The role manages validation engineers and specialists, oversees IQ/OQ/PQ and equipment lifecycle activities, ensures compliance with FDA, EU GMP, Annex 1, and ICH requirements, supports new product introductions and facility expansions, and leads deviations, CAPA, and risk-based validation efforts. Candidates should have a bachelor’s degree in a relevant field, at least five years of pharmaceutical validation experience, and at least one year in a supervisory or leadership role.
