Document Controller

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