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Job Title


Regulatory Publishing Associate


Company : Cpl Life Sciences


Location : maidstone, south east england


Created : 2025-09-10


Job Type : Full Time


Job Description

Job Title: Regulatory Publishing Associate – EU/ROW TeamLocation: Sandwich, Kent, UK - Hybrid (2–3 days on-site)Contract Type: Initial 12-month contract (PAYE, inside IR35)Start Date: ASAPAn 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@You MUST be based in the UK and be able to travel to the office 2/3 days per week.