Posted: 18 June
The role
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
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