Catalent
PreproductionCoordinator
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Preproduction Coordinator at Catalent. Skills: preparation of clinical trial packaging documentation, integrity and quality of clinical supplies. Prepare and generate study-specific clinical packaging documentation. Ensure all work is completed in compliance with GMP and relevant SOPs”
What You'll Achieve.
deliver high-quality outputs in line with regulatory and client requirements
What They're Looking For.
Must Have
Good level of English and Maths, Good written and verbal communication skills, Proficient in IT systems, including Word and Excel and be able to learn on site systems, The ability to work as part of a team, adopting a right first-time approach
What You'll Do.
Prepare and generate study-specific clinical packaging documentation
Ensure all work is completed in compliance with GMP and relevant SOPs
Maintain high quality standards
documenting deviations where required
Support the integrity and timelines of clinical trial supply packaging
How You'll Work.
Team & Collaboration
Work collaboratively with colleagues and management teams
Communication Scope
Good written and verbal communication skills
Full Job Description
**Pre Production Coordinator** * Monday to Friday, standard day hours, 37 hours per week * 100% onsite Our Bathgate location in Scotland, UK is an integral part of Catalent’s European clinical supply services network. This facility has a comprehensive range of capabilities to support sponsors’ studies throughout the UK, Europe and beyond, including clinical supply management, FastChain® demand-led supply, clinical-scale commercial packaging, and QP release services. We are looking for a **Preproduction Coordinator** to join our Clinical Supply Services team. This role plays a key part in supporting the preparation of clinical trial packaging documentation and ensuring the integrity and quality of clinical supplies. You’ll work closely with internal teams to deliver high-quality outputs in line with regulatory and client requirements, while contributing to a culture of continuous improvement. **The Role** * Prepare and generate study-specific clinical packaging documentation * Ensure all work is completed in compliance with GMP and relevant SOPs * Maintain high quality standards, documenting deviations where required * Support the integrity and timelines of clinical trial supply packaging * Work collaboratively with colleagues and management teams **The Candidate** * Good level of English and Maths * Good written and verbal communication skills * Proficient in IT systems, including Word and Excel and be able to learn on site systems * The ability to work as part of a team, adopting a right first-time approach **Why You Should Join Catalent:** * **Competitive Salary** – Reflecting your experience and skills. * **Benefits** – a pension scheme matching up to 7.5% and life assurance. Enjoy BUPA private medical insurance, a generous holiday entitlement that increases with tenure, and the option to trade leave. * **Career Development** – Access high-quality training, mentoring, and cross-functional opportunities within Catalent’s global network. Benefit from a subscription
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