Label Process Specialist

Catalent Pharma Solutions; Kansas City (MO); On-site; USD 45,000 - 60,000; Full time

Benefits offered by this job

PTO plus 8 holidays

Benefits from day one (medical, dental

Tuition reimbursement

Job summary

Catalent’s Kansas City facility is seeking a Label Process Specialist to manage the complete label lifecycle for clinical and commercial programs. You will work with project teams and suppliers to design, print, and verify labels that meet regulatory and client requirements.

Key duties include setting up study labeling, generating kit lists, producing multi-language labels, maintaining records, and troubleshooting printers. The role is onsite, with regular daytime hours.

Qualifications

• High School Diploma or GED required.
• Strong communication and problem-solving skills.
• Ability to read, write, and speak clear English.
• 2–4 years of labeling or pharmaceutical operations experience preferred.

Responsibilities

• Set up labeling study requirements using the Label Management Software.
• Generate kit lists for clinical protocols that meet study and distribution requirements.
• Import client-provided kit lists into the Label Management Software for use at Catalent.
• Coordinate with suppliers for the design and production of multi-page booklet labels.

Skills

Label management

Documentation

English communication

Education

High School Diploma or GED

Associate degree in business or related field

Tools

Label Management Software

GSA (Global Scan Assembly)

Job description

About Site

Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.

Position Summary

We have an opportunity for a Label Process Specialist to join our team. This position is responsible for generating and managing the entire label process from the Project Management team, ensuring on-time and accurate delivery of labels for all business unit label requirements. The role involves preparing, coordinating, designing, and generating clinical study and commercial labels, as well as managing kit lists and label printing activities. The successful candidate will work closely with project management and suppliers to ensure compliance with all regulatory and quality standards.

Shift: 8am-4:30pm M-F

Location: Kansas City, MO 100% Onsite

The Role

• Set up labeling study requirements using the Label Management Software.
• Generate kit lists for clinical trial protocols that meet client study and distribution requirements.
• Import client-provided kit lists into the Label Management Software for use at Catalent.
• Maintain accurate and complete records of kit numbers utilized by Catalent.
• Create packaging configurations in the Global Scan Assembly system (GSA).
• Create label print requests against approved kit list and label design specifications.
• Work closely with project management to ensure accurate timelines and labeling requirements.
• Generate and revise label proofs for client review and approval.
• Provide suggested label text layouts to meet client study needs.
• Approve label designs and perform peer reviews.
• Generate multi-language labels using appropriate labeling systems and regulatory references.
• Coordinate with suppliers for the design and production of multi-page labels (booklet labels).
• Clean, maintain, calibrate, and adjust printer settings; operate label printers and verify barcodes.
• Troubleshoot printer issues and manage vendor escalations and documentation.
• Order and maintain label inventory in conjunction with Supply Chain personnel.
• Verify PS/PR scope documents for accuracy and required approvals.
• Participate in project kick-off meetings to establish clinical trial design and label requirements.
• Manage and maintain logbooks for label design activities.
• Set up routers, create master bills of materials, and generate work orders for label printing.
• Allocate label lots to pick lists and manage label stock inventory based on client specifications.
• Perform other duties as assigned.

The Candidate Minimum Requirements

• High School Diploma or General Educational Development (GED).
• Ability to communicate effectively with engineers, technicians, customers, staff, and other personnel.
• Ability to troubleshoot simple to complex process and equipment problems.
• Demonstrated ability to plan and independently implement multiple projects.
• Strong problem-solving and analytical skills.
• Excellent written, verbal, and interpersonal communication skills, including the ability to present information.
• Blend knowledge and analysis with logic, active listening, and a continuing interest in simplification.
• Act ethically.
• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
• Willingness to share skills and information with others.
• Ability to read, write, and speak clear English.
• This role also requires 20/30 corrected vision exam and a colorblindness test.

Preferred Skills & Background

• Associate degree in business, Graphic Design, or a related field preferred.
• 2–4 years of clinical labeling or related pharmaceutical operations experience preferred.
• Strong computer and technical experience preferred.
• Proficiency in business computer applications such as word processing, spreadsheets, and database software preferred.

Why You Should Join Catalent

• 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.
• Personal initiative.
• Dynamic pace.
• Meaningful work.

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life‑saving and life‑enhancing products to patients around the world.

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities.

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 [e-mail]. 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.

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life‑cycle supply. With time-tested experience in development sciences, delivery technologies, and multi‑modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life‑enhancing and life‑saving treatments for patients annually.