Document Controller – 12‑Month Contract in Dublin

About the role

We are seeking an experienced Document Controller to join a leading multinational biopharma company in Dublin on a 12‑month contract. You will work client‑side, overseeing all project documentation throughout the lifecycle of a major facility development, gaining hands‑on experience with innovative equipment and large‑scale pharmaceutical operations.

Key responsibilities

• Control and manage all project documentation from receipt to archiving.
• Handle document review, approval, issue, revision control, and maintain accurate registers and trackers.
• Interface with EPCM partners, vendors, contractors, and internal stakeholders.
• Ensure all documentation complies with GMP, data‑integrity, and ALCOA principles.
• Support construction, commissioning, and qualification documentation activities.

Required profile

• Proven experience as a Document Controller on pharmaceutical or life‑science capital projects.
• Hands‑on experience using EIDA for document management.
• Background working client‑side or within an owner’s project team.
• Strong understanding of GMP documentation requirements.

Required skills

• EIDA document management system