- Esperienza
- Qualsiasi
- Stipendio
- EUR 50 – EUR 60 / hour
- Aperture
- 1
- Pubblicato
- 4 ore fa
- Work mode
- In ufficio
- Eligibility
- Experienced Document Controllers with a background in pharmaceutical or life sciences capital projects, especially those able to work on-site in Ireland and available immediately or at short notice, may apply.
- Resume
- Required to apply
Where you'll work
Descrizione del lavoro
Role Overview
This opportunity is for a client-side Document Controller based in Dublin on a fully on-site basis. The assignment is an initial 12-month contract supporting a biopharmaceutical capital project in North Dublin, with day rates of €50 to €60 per hour. Candidates who can start immediately or within a short notice period are preferred.
About the Assignment
You will join the client project team on a major pharmaceutical site-based capital project in Ireland. The position is embedded on site and focuses on managing governance and control of project documentation throughout design, construction, CQV, and handover stages.
Core Responsibilities
The role reports to the DC Director, Project Director, and Project Manager. You will oversee project document management systems, maintain document control quality, and ensure audit readiness from document creation through to project completion and handover. You will also coordinate registers and workflows for RFIs, submittals, documents, benchmarks, and RAMS, while leading the O&M manual handover process. The position includes working closely with construction management teams, contractors, consultants, and other stakeholders, as well as delivering system training and end-user support. Additional day-to-day tasks may be assigned as needed.
Requirements
Applicants should bring solid experience as a Document Controller on pharmaceutical or life sciences capital projects, with hands-on use of EIDA for document management. Prior work on the client or owner side is essential, along with a strong grasp of GMP documentation standards. Experience supporting documentation for construction, commissioning, and qualification activities is required. The role also requires the ability to work full time on an active pharmaceutical site in Ireland.
Preferred Experience
Experience on large Irish pharma projects such as drug product, biologics, or sterile manufacturing facilities will be viewed favourably. Familiarity with platforms such as ValGenesis, Kneat, ACC, or similar systems is also desirable.
Additional Information
This is a fully on-site role in Dublin. The contract length is 12 months and engagement can be via UMB or LTD. The client is seeking someone who is available immediately or on short notice.
Terms and Conditions
The role is being handled by an employment agency for recruitment and temporary worker supply. Any submission to the role is subject to the applicable terms, privacy policy, and disclaimers provided by the recruitment agency.