Regulatory Publishing Associate, nottingham
Client:
Cpl Life Sciences
Location:
nottingham, United Kingdom
Job Category:
Other
-
EU work permit required:
Yes
Job Views:
2
Posted:
22.08.2025
Expiry Date:
06.10.2025
Job Description:
Job Title: Regulatory Publishing Associate – EU/ROW Team
Location: Sandwich, Kent, UK - Hybrid (2–3 days on-site)
Contract Type: Initial 12-month contract (PAYE, inside IR35)
Start Date: ASAP
An exciting opportunity to join a leading pharmaceutical company on an initial 12-month basis. Are you detail-oriented, proactive, and ready to contribute to a high-impact regulatory project? Join a dynamic EU/ROW publishing team supporting global health authority submissions. This team of 10 professionals—both contractors and full-time employees—collaborates on dossier publishing across diverse formats and regional requirements, including eCTDs, eSubs, and NeeS.
About the Role:
Due to an exciting transition to a new Regulatory Information Management (RIM) system in 2026, we’re seeking additional support to maintain business-as-usual (BAU) portfolio activities and ensure timely delivery of submissions.
You’ll be involved in:
* Preparing and publishing regulatory dossiers for submission to health authorities.
* Navigating varying regional and format-specific requirements.
* Collaborating with team members to troubleshoot and streamline publishing processes.
Requirements:
* Has prior experience in regulatory publishing or a related field.
* Is familiar with tools such as Adobe Acrobat, ISI Toolbox, MS Excel, Lorenz, and RIM systems.
* Demonstrates a systematic, detail-driven approach to work.
For more information, please reach out to me at lucy.kirkaldy@cpl.com
You MUST be based in the UK and be able to travel to the office 2/3 days per week.
Please note that if you are NOT a passport holder of the country for the vacancy you might need a work permit. Check our Blog for more information.
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Created on 22/08/2025 by JR United Kingdom
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