Lead Equipment Validation Supervisor - Sterile/GMP
Hikma Pharmaceuticals
Hikma Pharmaceuticals in Bedford, Ohio is looking for an experienced Equipment Validation Supervisor. This role will lead the qualification and validation activities for sterile and injectable manufacturing environments, ensuring compliance with FDA and global standards. The ideal candidate should have over 5 years of validation experience and be skilled in managing a team. The position offers a full-time opportunity with competitive compensation and comprehensive benefits. #J-18808-Ljbffr Hikma Pharmaceuticals
Vacancy posted 1 day ago
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