Label Specialist
Listed on 2026-10-11
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Manufacturing / Production
Quality Engineering, Production QC/QA -
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Quality Engineering, Production QC/QA
Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.
Position SummaryWe have an opportunity for a Label Specialist to join our team supporting the Project Management Team, Operations Team, and our customers. This role involves printing and inspecting labels for clinical and commercial packaging and distribution. Work is performed in compliance with regulatory requirements, good manufacturing practices, and standard operating procedures. The position requires attention to detail, documentation accuracy, and collaboration across teams to ensure quality and compliance.
Shift: 2:30pm-11pm M-F
Location:
Kansas City, MO
100% Onsite
The Role- Maintain, manage, and request logbooks accurately for inspecting labels in label control.
- Complete and manage documentation and paperwork for label creation and inspection.
- Inspect English text, foreign text, multiple panel, and commercial labels for accuracy.
- Review and approve randomization logs for accuracy.
- Understand blinding requirements and inspect labels accordingly.
- Maintain and request logbooks for printing labels, ensuring awareness of space and equipment logbooks.
- Calibrate and adjust printer settings; set up and use Printronix and Zebra printers correctly.
- Clean and maintain Printronix and Zebra printers per standard operating procedures.
- Understand printer ribbons and their appropriate uses.
- Run print jobs, verify barcodes, and generate reprints and required paperwork.
- Perform other duties as assigned.
- High-school diploma or General Educational Development (GED).
- 0–3 years of clinical labeling experience.
- Ability to communicate effectively with project management, engineers, customers, and staff.
- Ability to plan and independently implement multiple projects.
- High attention to detail and excellent documentation skills.
- Strong problem-solving and analytical abilities.
- Excellent written, verbal, and interpersonal communication skills.
- Ability to interpret various instructions in written, oral, diagram, or schedule form.
- Willingness to share skills and information with others.
- Team-oriented approach to achieve results.
- This role also requires 20/30 corrected vision and a colorblindness test.
- Demonstrated ability to read, write, and speak clear English.
- Experience in a Good Manufacturing Practice (GMP) environment preferred.
- Proficiency in business computer applications such as word processing, spreadsheets, and database software.
- Defined career path and annual performance review and feedback process.
- Diverse, inclusive culture.
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
- Competitive paid time off plus 8 paid holidays.
- Community engagement and green initiatives.
- Medical, dental, and vision benefits effective day one of employment.
- Tuition reimbursement.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to Disabili This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
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