Force is seeking an experienced Document Controller to join their team on a major Biopharmaceutical project in Ireland. The role ensures client-side control of all project documentation across design, construction, and handover phases. Responsibilities include managing documentation, ensuring compliance with GMP requirements, and supporting audits and project close-out activities. Candidates must have proven experience in pharmaceutical capital projects and be able to work full-time on-site in Dublin. This is a 12-month contract position.
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