Quality Management Assistant

Role: Support quality systems and regulatory compliance within a pharmaceutical distribution center, ensuring distribution activities adhere to cGMP and FDA regulations. Responsibilities: assist with preparing and reviewing batch documentation (COA, compliance reports, temperature data), support inventory classification and control, manage customer returns in line with SOPs, facilitate shipping studies to maintain product integrity, and perform sampling activities per SOPs. Also support internal and regulatory audits through documentation review and preparation. Requirements: High School diploma or GED; 2+ years in pharmaceutical distribution or QA; proficiency in Microsoft Office; strong understanding of FDA regulations and cGMP; ability to read/write in English. HighValue: pharmaceutical distribution, QA, cGMP compliance, FDA regulation familiarity, documentation and audit support. WorkSetup: not specified; likely on-site given the operational nature.