Description
New Build Biopharma plant have an URGENT & LONG TERM CONTRACT requirement for an experienced Document Controller.Ideally, we are looking for candidates with 3-5 years Documentation experience who can start within 4 weeks on site in Dublin. Excellent opportunity to join this €700 million New build facility currently in detailed design.
Working within the Client team duties will include:
- Manage the review and approval cycle of Systems Development life cycle documents.
- Ensure all comments are collated and returned per the schedule.
- Manage the routing/approval on the internal document approval system.
- Liaise with Systems Integrator, and other technical vendors to ensure documents are routed in a timely manner and to the correct people.
- Coordinate automation document deliverables with the CSV Lead and wider C&Q team.
- Document Control experience within a regulated environment.
- Highly organised and methodical.
- Strong knowledge of Sharepoint, Word and Excel.
- Pharma/GxP experience, essential.
- Proactive and can work on own initiative.
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