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. Position Summary We have an opportunity for an Associate Scientist to join our team. In this role, you will manage multiple responsibilities to ensure tasks are prioritized and completed on time. You will assist in the design, coordination, and execution of development and clinical trial material activities, including formulation and data interpretation. You will also support documentation, problem-solving, and maintain communication with internal teams, vendors, and occasionally clients. This position plays a key role in supporting departmental and corporate objectives. Shift: Monday - Friday, 8am - 9pm Location: Greenville, NC 100% Onsite
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Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree