Catalent’s Winchester, KY site is the company’s flagship U.S. manufacturing location for large‑scale oral solid dose forms, operating from a 180,000‑square‑foot facility with fully integrated development and analytical services. The site specializes in complex and controlled‑release oral dose technologies, supporting product development, technology transfer, and commercial manufacturing across pharmaceutical and consumer health programs. Winchester has a long commercial manufacturing track record, having launched 100+ products and producing billions of tablets and capsules annually, making it a critical site within Catalent’s oral dose network. Position Summary We have an opportunity for a QA Analytical Auditor to join our team. This role supports the release of all materials from the quality control lab and ensures compliance with technical and analytical requirements. You will manage your time effectively, work with minimal direction, and handle a wide range of high-visibility tasks. The position involves reviewing data for GMP compliance, supporting investigations, and participating in audits to maintain quality standards. Shift: Monday-Friday 8 AM - 5 PM Location: Winchester, KY 100% Onsite
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Job Type
Full-time
Career Level
Mid Level