Quality Investigations Lead (GMP, CAPA)
Catalent Pharma Solutions
Catalent’s Greenville, North Carolina site seeks a Production Event Investigator to author and oversee deviations, investigations, and CAPAs under GMP frameworks. You will partner with cross-functional teams to identify root causes and ensure timely corrective actions in a fast-paced pharmaceutical setting. The role requires collaborating across Commercial Operations, Packaging, Pharmaceutical Development, and labs, with on-site work M–F, 8:00am–5:00pm in Greenville, NC. #J-18808-Ljbffr Catalent Pharma Solutions
Vacancy posted 1 day ago
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