Document Controller

Job Description Document Controller Location: Dublin, Ireland (Onsite) Contract Duration: 12-month contract Rate: 60.00 Hourly Step into a pivotal client-side role where your expertise in pharmaceutical documentation drives the success of cutting-edge projects in Ireland's thriving life sciences sector. Key Responsibilities Client-side control of all project documentation across the full lifecycle Manage document receipt, review, approval, issue, revision control and archiving Interface with EPCM partners, vendors, contractors and internal stakeholders Ensure documentation complies with GMP, data integrity and ALCOA+ principles Maintain accurate document registers, trackers and status reports Support CQV documentation, executed protocols and final turnover to operations Support audits, inspections and project close-out activities Essential Experience & Requirements Proven experience as a Document Controller on pharmaceutical or life sciences capital projects Essential: hands-on experience using EIDA for document management Experience working client-side or within an owner's project team Strong understanding of GMP documentation requirements Experience supporting construction, commissioning and qualification documentation Ability to work full-time on a live pharmaceutical site in Ireland Experience on large-scale Irish pharma projects (drug product, biologics, sterile facilities) Familiarity with ValGenesis, Kneat, ACC or similar platforms Don't miss this opportunity to take ownership of critical pharmaceutical documentation - apply now and be part of Ireland's leading life sciences projects!