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Catalent

Global contract drug formulation, manufacturing, packaging

Label Specialist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeKansas City, MO, USANo salary listed

About the Job

Requirements

  • A high-school diploma or GED is required.
  • Zero to three years of clinical labeling experience is required.
  • Ability to communicate effectively with project management, engineers, customers, staff, and other personnel.
  • Ability to plan and independently implement multiple projects.
  • High level of attention to detail.
  • Strong documentation skills.
  • Strong problem-solving and analytical skills.
  • Ability to interpret instructions furnished in written, oral, diagram, or schedule form.
  • Ability to share skills and information with others and foster teamwork to achieve results.
  • Corrected vision of 20/30 and successful completion of a colorblindness test are required.
  • Ability to read, write, and speak clear English.

Responsibilities

  • Maintain, manage, and request logbooks accurately for inspecting labels in label control.
  • Handle documentation and paperwork for the creation and inspection of labels.
  • Inspect English text, foreign text, multiple-panel, and commercial labels for accuracy.
  • Review and approve the accuracy of prepared randomization logs.
  • Understand blinding requirements and inspect labels for accurate blinding.
  • Maintain, manage, and request logbooks for printing labels in label control, with awareness of space and equipment logbooks.
  • Calibrate and adjust printer settings; set up and use Printronix and Zebra printers.
  • Clean and maintain Printronix and Zebra printers according to standard operating procedures.
  • Understand printer ribbons and their specific uses.
  • Print job runs, verify barcodes, and generate reprints and required paperwork.

Desired Qualifications

  • Experience in a good manufacturing practice (GMP) environment is preferred.
  • Proficiency in business computer applications, including word processing, spreadsheets, and database software, 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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