QA Compliance Specialist GMP, Audits & Regulatory Impact
Hikma Pharmaceuticals
Hikma Pharmaceuticals in Bedford, Ohio is seeking a Specialist, QA Compliance to support Quality Group initiatives by ensuring adherence to regulatory compliance and company policies. Responsibilities include overseeing customer complaints and audits, supporting inspection readiness, and developing quality training. The ideal candidate has a Bachelor of Science in a scientific discipline, along with 3-5 years of relevant experience in the pharmaceutical industry, focusing on quality systems and compliance. The position offers a comprehensive benefits package. #J-18808-Ljbffr
Vacancy posted 4 days ago
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