LSC have a great contract opportunity for Engineering Document Control Specialist to join a Cork based Biopharmaceutical company. The site manufactures low volume bulk API for Phase III clinical trials, initial product launch and long-term market support. The team on site grow, purify, formulate, and bulk fill mammalian cell culture derived APIs for medicines intended for human use. ABOUT THE PROJECT - KEY RESPONSIBILITIES: Control and maintenance of the Engineering Documentation Control Centre. Control, issuance and archiving of Project & Site Drawings. Control and issuance of the numbering system for Commissioning & Restart Documents. Prepare and draft controlled documents through Veeva and Track wise. Any other duties as assigned by the Core Projects Manager, in relation to engineering document control. Circulation of Project Engineering transmittals. Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply Apply via this advert or contact Grinne Hodnett at LSC on if you have any more questions about this opportunity Skills: GMP Document Control edocs quality agreements