Document control specialist is required for a biopharma facility in Cork. The Engineering Document Control Specialist will report to the Core Projects Manager and is responsible for the control of the engineering documentation system. Initially a 12-month contract. 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 Trackwise. Any other duties as assigned by the Core Projects Manager, in relation to engineering document control. Circulation of Project Engineering transmittals. Maintenance of Engineering Registers. Ensuring compliance within Engineering for removal of documentation from the Engineering Documentation Control Centre Control of Engineering documents and Vendor documents to and from the Engineering Documentation Control Centre. Archival of Engineering documents and logbooks Other duties as assigned Requirements A Bachelor's Degree in the relevant technical field 1-2 years' industry experience in a GMP environment Strong written and verbal communication skills, with a keen eye for detail Skills: GMP Bsc Veeva Trackwise
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