Document Controller, Old Connaught

Role Title: Document Controller Role Type: 12 Month Contract Location: Dublin 15 We are seeking an experienced Document Controller to join the client project team on a major Biopharmaceutical site-based capital project in Ireland. The role is fully embedded on site and responsible for the client-side control and governance of all project documentation across design, construction, CQV and handover phases.

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

Fully on site role.

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