QC DOCUMENTATION COORDINATOR

QC Documentation Coordinator – Ireland – Contract Do you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than people.
They are looking to add to their team and require a QC Documentation Coordinator.
This a fantastic opportunity to be involved with the critical investment projects both on-site and remotely.
Essential Duties and Responsibilities for this role include, but are not limited to, the following.
Be a document system expert for the Quality Control Department; this will include document generation and review and document system work-flow expedition where applicable - examples include Standard Operation Procedures, Work Instruction, Policies, Safety procedures, Annual Product Reviews, electronic logs.
Format, write and deliver necessary documentation in line with Merck Global Policies, Procedures and Guidelines, regulatory requirements.
Support laboratory administration activities through documentation generation, documentation filing, tracking and auditing.
Manage and complete department specific assignments, including periodic review of documents.
Support continuous improvement by active participation and engagement with laboratory team for document updates out of investigations and corrective actions.
Contribution to Kaizen events and documentation improvement projects as appropriate.
Desirable Experience.
Experience and/or a particular skill set in their area of expertise that adds value to the Business, preferably GMP setting.
Degree preferred, ideally in a related discipline  Understanding of Lean Six Sigma Methodology preferred If this role is of interest to you, please apply now!