Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development through commercial manufacturing and packaging. The site specializes in oral solid dosage forms, supported by integrated formulation expertise, comprehensive analytical services, and scalable manufacturing capabilities designed to support both commercial products and potent or targeted therapies, including orphan drugs. Backed by more than $100 million in recent investments, the Greenville operation features fit‑for‑scale infrastructure, potent handling capabilities, and a strong regulatory track record, making it a critical part of Catalent’s global network for advancing complex oral drug programs from development to market. We have an opportunity for a Principal Quality Associate, Supplier Audits, to join our team. This role involves performing and facilitating system-based audits and risk assessments for Supplier Audits and Internal Quality Systems. You will support both non-commercial and commercial audits as well as the Inspection Readiness Program. The position requires strong organizational skills to manage audit schedules, ensure compliance, and maintain quality standards across the organization. Shift: Monday- Friday, 8:00am-5:00pm Location: Grenville, NC 100% Onsite
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Job Type
Full-time
Career Level
Senior