LSC have a great contract opportunity for a Document Controller to join a Biotech Drug Substance Manufacturing Facility in Munster.
If you have at least 3 years of relevant experience in a cGMP environment and ready for your next challenge, this could be the perfect project for you!
Main Purpose and Objectives of the Position:
- As a Document Controller, you will be responsible for electronic documentation and records management oversight
- This role is responsible for execution, maintenance, and administration of document management systems.
- The Document Controller will aid in initial program startup and routine operation of the site, as well as support site inspection readiness and execution.
- The Document Controller will aid in start-up and routine operation of the document and records management program execution in particular:
- Document management including metadata
- Revision and Change control
- Quality Systems support
- Audit support
- Records Management
Preferred but not required:
- Ability to create prototype implementations to test documentation accuracy and effectiveness
- Experience working in Document control in a GMP environment.
Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a valid Stamp 1G/Stamp 4 visa to apply!
Apply via this advert or contact Siobhan Cummins at LSC on 021-4777329 or at if you have any more questions about this opportunity!
