Overview
Quality Admin Jobs in Lexington, Kentucky, USA at Neogen
Neogen Corporation is seeking a Quality Administrator to join our team. In this role, you will play a critical part in supporting our production and quality processes by maintaining documentation, ensuring compliance with ISO and cGMP standards, and assisting with quality audits. The ideal candidate will have a strong background in quality assurance, document management, and compliance, with excellent attention to detail.
This role follows an onsite model to accommodate business needs while maintaining team collaboration.
Essential Duties and Responsibilities:
Maintain and manage quality documentation, including batch records, training logs, validation reports, and compliance documentation.
Ensure adherence to ISO 9001, cGMP, and company quality standards.
Audit records to verify accuracy, completeness, and compliance with internal policies and external regulations.
Compile and analyze quality data to support process improvements and trending programs.
Assist in the release and verification of raw materials used in production.
Support manufacturing and quality teams by ensuring accurate documentation and traceability.
Collaborate with cross-functional teams to uphold quality assurance processes.
Education and Experience:
1–3 years of experience in quality assurance, document management, or a related field, preferably in a regulated environment.
Experience with ISO 9001 standards and quality documentation processes preferred.
Proficiency in Microsoft Office and quality management software.
Please press Apply to submit your application.
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Title: Quality Admin
Company: Neogen
Location: Lexington, Kentucky, USA
Category: Quality Assurance – QA/QC (Quality Control / Manager, Quality Technician/ Inspector, QA Specialist / Manager, Quality Engineering)
