Job Description
Responsible for supporting the Quality Control Department in the management of external sample shipments and retain sample management. Support various administrative duties associated with sample management, ensuring that objectives are effectively achieved to ensure compliance, safety, and reliable supply to our customers. This is a day role based on site (Mon-Fri).
11-month contract role with salary dependent on experience.
Functions
1. Act as point of contact for QC sample and retain management.
2. Responsible for QC external sample management from receipt to shipment.
3. Responsible for QC retain sample management from receipt to disposal.
4. Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC Laboratory and ability to identify gaps in processes or systems.
5. Proficient with Microsoft Office applications (Outlook, Excel, Word, and PowerPoint).
6. Proficient with Lab management software system (LIMS).
7. Prepare documents and coordinate sample movement within the Warehouse area.
8. Review eLogs and/or LIMS to align physical quantities of samples in freezers/refrigerators/lean lifts and sample cages.
9. Take ownership of processes related to sample handling, e.g., oversight of freezers/refrigerator clean schedule.
10. Perform or support sample management-related non-conformance investigations.
11. Support internal and regulatory audits.
12. Format, write, and deliver necessary documentation in line with global policies, procedures, and guidelines, and regulatory requirements.
13. Support continuous improvement by active participation and engagement with the laboratory team during investigations and subsequent corrective actions.
14. Ensure timely completion of all assigned documents to meet site metric requirements.
15. Work collaboratively to drive a safe and compliant culture in Carlow.
16. Participate in QC daily tier meetings and ensure effective communication of assigned tasks/projects.
Experience
Technical:
1. Proficiency in Microsoft Word, Office, Excel, and job-related computer applications required, i.e., LIMS.
2. Knowledge of regulatory/code requirements to Irish, European, and International Codes, Standards, and Practices.
3. Understanding of Lean Six Sigma Methodology preferred.
Qualifications
1. Education: Third level qualification preferred, ideally in a related discipline.
2. Experience: Particular skill set in their area of expertise that adds value to the business, preferably in a GMP setting.
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