Preproduction Coordinator FTC (Label Design)

Preproduction Coordinator FTC (Label Design)

Preproduction Coordinator FTC (Label Design)

Location: Bathgate, United Kingdom

Time Type: Full Time

Posted On: Posted Yesterday

End Date: May 1, 2025 (11 days left to apply)

Job Requisition ID: 0088444

Bathgate is currently recruiting a Preproduction Coordinator (Label Design) to join the preproduction department on a 14 month FTC.

As part of the label design team within the Preproduction department, you will take text in various languages to produce appropriately sized and professionally designed layouts of clinical trial labels that will then be applied to patient kits used in clinical trials. You will be required to work with multiple documents as well as label design software. It is essential that candidates have good attention to detail, can multitask and work to strict deadlines and can adapt to changing priorities in a fast-paced environment.

The role:

• Keep up to date with industry best practice.
• Maintain high quality standards ensuring all deviations are documented as required.
• Report to your Line Manager any issues which may impact on the quality or timelines specified for the packaging of supplies.
• Maintain a personal training record and attend training sessions as required and a high standard of Good Housekeeping in all working areas.
• Competently perform tasks as detailed by the Label Control skills matrix.
• Undertake other tasks as assigned by relevant Manager(s).
• Participate in the implementation of any new systems or upgrades to systems pertaining to Label Control department and any process improvement initiatives to support Label Control department, Bathgate site or wider Catalent organisation, as appropriate.
• Build and maintain an organised and disciplined Label Control department.
• Design labels to meet Catalent, Client, Study and Regulatory requirements.
• Request regulatory services and translations.
• Follow safety and manual handling guidelines set by EHS and COSHH.
• Complete documentation in accordance to relevant SOPs and to comply with GMP.

The candidate:

• Strong attention to detail.
• Previous experience working within a GMP environment (advantages).
• Confident user of Microsoft packages, including Word and Excel.
• Administration skills.

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.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.

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 DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability.