Filling Technician

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.

Summary The Filling Technician is responsible for the safe, compliant, and efficient execution of pharmaceutical filling and packaging activities. The position supports commercial, development, scale-up, and Clinical Trial Material (CTM) packaging and filling operations in accordance with approved batch documentation, SOPs, work instructions, and cGMP requirements. The Technician performs equipment setup and operation, changeovers, in-process checks, cleaning, material handling, and documentation with minimal supervision. The role requires technical aptitude, attention to detail, sound judgment, and accountability for assigned activities. Shift: Monday- Friday 8:00am-5:00pm Location: Greenville, NC 100% Onsite The Role Perform filling and packaging activities in accordance with approved batch documentation, SOPs, and work instructions Set up, operate, change over, clean, and maintain assigned packaging equipment and support line clearance and equipment readiness activities Support various packaging and filling technologies and operations as required by business needs Recognize abnormal equipment or process conditions and promptly communicate issues that may affect safety, quality, compliance, or production Perform required in-process checks, inspections, testing, and equipment verifications in accordance with established requirements Verify product and packaging attributes, identify and segregate unacceptable product or components, and support Right-First-Time execution Maintain the work area and equipment in a clean, organized, and inspection-ready condition; Stop work and escalate conditions that may compromise product quality, safety, or compliance Accurately complete and verify batch records, logbooks, inventory transactions, forms, and other required documentation in compliance with cGMP and data integrity requirements, ensuring the accuracy of materials, components, quantities, identification, and status information, and promptly reporting any discrepancies, errors, or questionable entries to the appropriate Team Lead or Supervisor Collaborate effectively with cross-functional teams to support safe and efficient packaging operations Communicate equipment issues, material shortages, process abnormalities, and execution barriers in a timely manner Other duties as assigned The Candidate Minimum Requirements High school diploma or equivalent required, with at least five years of pharmaceutical manufacturing or packaging experience in an oral solid dosage facility Experience working in a regulated environment with strong documentation practices, including batch records and logbooks Hands-on experience with filling (e.g. API-in-capsule) and packaging equipment and the ability to follow detailed instructions and in-process requirements Demonstrated ability to work independently, recognize abnormalities, and appropriately escalate issues Strong attention to detail, mechanical aptitude, and ability to learn and operate packaging and equipment Ability to perform basic mathematical calculations and accurately record results Position requires the ability to lift 40 lbs unassisted, and push and pull in excess of 100