The Analytical Chemist I primarily performs routine analytical testing in support of pharmaceutical products, following applicable safety, quality, and regulatory requirements. The role supports the development and manufacturing of high-quality pharmaceutical products in a collaborative, compliance-driven environment. It is based 100% onsite at Catalent’s Greenville, North Carolina site and follows a Monday–Friday, 8:00 a.m.–5:00 p.m. schedule. Under general supervision, the role performs routine chromatographic and spectrophotometric analyses for pharmaceutical excipients, active pharmaceutical ingredients (APIs), and/or drug products. Testing may include assays such as potency, related substances, residual solvents, and metals; dissolution; moisture; identification; and other wet-chemistry measurements. Common techniques and equipment include HPLC, GC, titrations, UV, and IR. The chemist maintains data integrity and good documentation practices, compares results with specifications and trends data where applicable, and ensures calibration standards and instrumentation are used, cared for, and returned properly. The role follows approved methods, standards, and internal SOPs to support accurate testing and prevent repeat testing, deviations, and investigations. Data is entered into established reports, templates, or software systems. Other duties may be assigned.
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Job Type
Full-time
Career Level
Entry Level