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Catalent

Global contract drug formulation, manufacturing, packaging

Distribution Coordinator

Logistics & TransportationConfirmed live in the last 24 hours
Full-timeKansas City, MO, USANo salary listed

About the Job

Requirements

  • A high school diploma and at least 2 years of relevant industry or comparable experience are required.
  • Experience with enterprise resource planning systems is required; JD Edwards experience is preferred.
  • Strong project management and customer service skills are required.
  • Ability to maintain attention to detail while managing multiple priorities under tight deadlines is required.
  • Computer skills, including Microsoft Office, and ability to learn new systems quickly are required.
  • Ability to read, write, and speak clear English is required.
  • Ability to interpret written, oral, diagram, or schedule instructions is required.
  • Strong mathematical and reasoning ability is required.

Responsibilities

  • Coordinate and dispatch shipments of clinical trial material to clinical sites.
  • Process orders and assemble folders generated on-site and offshore.
  • Audit folders for accuracy against customer requests and source documentation.
  • Support same-day, 24-hour, 48-hour, bulk, sample, and Just-in-Time order requests.
  • Complete 95% of work to floor the day before and meet shift processing expectations.
  • Verify billing codes for accuracy.
  • Identify and resolve distribution issues related to operations, systems, processes, or technology.
  • Collaborate with Distribution Project Coordinators to resolve issues.
  • Enter Right First-Time data to track and trend downtime codes.
  • Understand customer expectations and execute work in alignment with the agreed scope of services.
  • Maintain the distribution group mailbox and documentation in compliance with GxP standards.
  • Support the distribution execution group in resolving operational and documentation issues.
  • Work with Quality, IT, Inventory, and other Supply Chain functions to resolve distribution issues.
  • Coordinate with Import/Export and Distribution Project Coordinators on international order processing and documentation.
  • Use source documentation, including the Distribution Summary and Distribution Master Checklist, according to Catalent standards.
  • Ensure study drug shipments comply with applicable standard operating procedures and customer-approved protocols.
  • Acknowledge shipment dispatch in IVRS when required.
  • Generate shipment documents for requested Clinical Trial Materials.
  • Support investigations and resolve customer issues related to distribution.
  • Perform other duties as assigned.

Desired Qualifications

  • An associate’s degree is preferred.
  • Experience in distribution and cold-chain operations is preferred.
  • Knowledge and experience in current Good Manufacturing Practices and Food and Drug Administration regulations are preferred.
  • Knowledge of exporting clinical trial materials is preferred.

About the Company

Catalent

Global contract drug formulation, manufacturing, packaging

Catalent provides end-to-end contract development and manufacturing services for pharmaceutical, biotechnology, and consumer health products. Its offerings cover drug formulation, large-scale manufacturing, clinical supply, and packaging under long-term partnerships, coordinating through a connected supply chain to move products from development to market. It differentiates itself with a broad, integrated service platform and long-standing customer relationships that help clients accelerate development and ensure reliable supply. The company aims to help clients bring products to market efficiently while balancing quality, cost, and sustainability across the product lifecycle.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Franklin Township, NJ
Founded
1996

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