Job Description
**Job Summary** Support Quality Control Department in laboratory GMP documentation management and administrative duties, ensuring compliance, safety, and reliable supply to customers. **Job Description** We are seeking a skilled professional to join our team as a Quality Control Document Specialist. The successful candidate will be responsible for supporting the Quality Control Department in the management of laboratory GMP documentation and administrative duties. **Key Responsibilities** * Be a document system expert for the Quality Control Department, including document generation, review, and workflow expedition * Format, write, and deliver necessary documentation in line with company Global Policies, Procedures, and Guidelines, regulatory requirements * Support laboratory administration activities through documentation generation, 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 * Contribute to Kaizen events and documentation improvement projects as appropriate * Ensure timely completion of all assigned documents to meet site metric requirements * Work collaboratively to drive a safe and compliant culture on site * Participate in QC daily meetings and ensure effective communication of assigned tasks/projects **Requirements** * Degree preferred, ideally in a related discipline * Experience and/or a particular skill set in their area of expertise that adds value to the Business, preferably GMP setting * Proficiency in Microsoft Word, Office, Excel, and electronic data management systems * Knowledge of regulatory/code requirements to Irish, European, and International Codes, Standards, and Practices * Report, standards, policy writing skills required * Understanding of Lean Six Sigma Methodology preferred * Skills: Word, Excel, Lean Six Sigma