Global CDMO manufacturing 60B+ doses annually across 40+ sites
Catalent operates a large-scale contract manufacturing footprint executing over 1,000 active development programs and launching 100+ new products annually. The tech stack is heavily weighted toward manufacturing execution (PLC, HPLC, UPLC, GCP, MES via Protheus) and enterprise resource planning (SAP, JD Edwards), with recent adoption of LabVantage for lab data management — signaling investment in digital compliance and traceability for GMP environments. The hiring mix is dominated by manufacturing and operations roles, with active project focus on formulation development, process optimization, and equipment qualification, reflecting a business scaling production capacity and operational rigor.
Notable leadership hires: Batch Record Lead, Account Director, Automation Project Lead, Finance Director, Operations Director
Catalent is a publicly traded contract development and manufacturing organization (CDMO) serving pharmaceutical, biotech, and consumer health companies globally. The company operates over 40 manufacturing sites worldwide, supporting approximately half of all FDA approvals over the past decade and producing over 60 billion doses annually. Core competencies span formulation development, biologics, gene therapy, drug delivery, and multi-modality manufacturing. The organization manages over 1,000 concurrent development programs and launches 100+ new products and line extensions per year. Catalent operates an international footprint with active hiring across nine countries, including major presence in the United States, Brazil, Germany, and Singapore.
PLC, HPLC, UPLC, GCP for manufacturing execution; SAP and JD Edwards for ERP; Protheus for MES; recently adopting LabVantage for lab data management and GMP compliance tracking.
Over 40 global sites with active hiring across nine countries: United States, Brazil, Germany, France, Canada, United Kingdom, Singapore, Argentina, and Italy. Headquarters in Tampa, Florida.
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