Teams at Catalent, Inc.

Reviews GMP and analytical testing documentation to support release of raw materials, in-process materials, and finished products. Reads and evaluates test methods, participates in customer and agency audits, assists with laboratory investigations and QC analyst training, and drafts or reviews SOPs, CAPAs, and audit responses. The role requires strong Empower software knowledge, laboratory safety expertise, scientific training, and the ability to manage multiple quality activities onsite under production deadlines.

Supervise pharmaceutical production activities on an overnight shift, ensuring safety, quality, delivery, cost, GMP, and SOP compliance. Train and support production personnel, manage staffing and performance issues, maintain payroll records, allocate resources, drive productivity and continuous improvement, reduce deviations, improve first-pass quality, support investigations and batch record revisions, and collaborate with cross-functional teams to meet production schedules.

Leads financial planning, budgeting, forecasting, reporting, and strategic analysis for a manufacturing business unit. Develops financial models and performance metrics, evaluates commercial and operational decisions, monitors revenue, margins, SG&A, EBITDA, and capital metrics, and identifies opportunities to reduce costs and improve profitability. Supports business reviews and communicates financial insights to decision-makers.