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
Desirable
· 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!
