Qc Sample Co Ordinator Job In Carlow

QC Sample Co-Ordinator role for a Pharmaceutical company in Carlow, Ireland, with an 11-month contract and potential for extension, requiring a strong understanding of GMP and laboratory management.

**Job Description**

**Company:** Pharmaceutical company in Carlow, Ireland

**Job Title:** QC Sample Co-Ordinator

**Duration:** 11-month contract with potential for extension

**Location:** Carlow, Ireland

• Act as point of contact for sample management in the QC Laboratory
• Responsible for QC sample management from receipt to disposal
• Knowledge and understanding of current Good Manufacturing Practices (c GMP) related to the QC Laboratory
• Identify gaps in processes or systems

**Key Responsibilities:**

• Sample Coordinator will act as point of contact for sample management in the QC Laboratory
• Responsible for QC sample management from receipt to disposal
• Knowledge and understanding of current Good Manufacturing Practices (c GMP) related to the QC Laboratory
• Identify gaps in processes or systems
• Proficient with using Microsoft Office applications (Outlook, Excel, Word, and Power Point)
• Proficient with Lab management software system (LIMS)
• Prepare documents and coordinate Sample movement within the Laboratory
• Review e Logs and/or LIMs to align physical quantities of samples in freezers/refrigerators
• Take ownership of processes related to sample handling
• Perform or support sample management related non-conformance investigations
• Supports Internal and Regulatory Audits
• Support continuous improvement by active participation and engagement with laboratory team
• Ensure timely completion of all assigned documents to meet site metric requirements
• Work collaboratively to drive a safe and compliant culture
• 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