- 経験
- どれでも
- 給料
- —
- 求人情報
- 1
- 投稿済み
- 8時間前
- Work mode
- 在任中
- Eligibility
- Professionals with document control experience in pharmaceutical, life sciences, or capital project environments, especially those familiar with client-side project teams and EIDA, may apply.
- Resume
- Required to apply
Where you'll work
仕事内容
Role overview
This position is for a Document Controller in Dublin, Ireland, supporting a 12-month contract with a multinational organisation in the biopharma sector. The role sits on a major facility development project and offers exposure to modern pharmaceutical technologies, large-scale operations, and innovative equipment within a fast-growing life sciences environment.
Key responsibilities
- Oversee project documentation from the client side throughout the entire project lifecycle.
- Handle the intake, review, approval, release, revision tracking, and long-term filing of documents.
- Work closely with EPCM partners, suppliers, contractors, and internal teams to keep documentation aligned.
- Make sure records meet GMP requirements, data integrity standards, and ALCOA principles.
- Keep document logs, trackers, and progress/status reports accurate and up to date.
Requirements
- Demonstrated background as a Document Controller on capital projects in pharmaceuticals or life sciences.
- Practical, hands-on experience with EIDA document management software is required.
- Previous exposure to client-side or owner’s team environments is important.
- Solid knowledge of GMP documentation expectations is needed.
- Experience handling documentation for construction, commissioning, and qualification activities is expected.
Additional information
This is a 12-month contract based in Dublin, County Dublin, Ireland. The opportunity is suited to someone looking to strengthen their experience on a major biopharma facility project while working with advanced equipment and modern pharma processes.
Call to action
Applicants who want to contribute to a high-profile project can proceed with their application.