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QC Sample Coordinator

Posted on:
October 7, 2024

The Highlights:

  • Excellent professional development and progression opportunities
  • Perform day to day laboratory testing & data review
  • Work with leading edge technology

The Role:

Elusav Recruitment have an incredible opportunity with a leading global Pharma and Biopharma company who is seeking a QC Sample Coordinator in Carlow, Ireland.

As the QC Sample Coordinator you will be responsible for supporting the Quality Control Department in the management of laboratory sample handling and various administrative duties associated with sample management.

Job 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
  • Prepare documents and coordinate Sample movement within the Laboratory.
  • Review eLogs and/ or LIMs to align physical quantities of samples in freezers/refrigerators.
  • Take ownership of processes related to sample handling e.g. oversight of freezers/refrigerator clean schedule.
  • Perform or support sample management related non-conformance investigations.
  • Supports Internal and Regulatory Audits.
  • Format, write and deliver necessary documentation in line with Company's Policies, Procedures and Guidelines, regulatory requirements.
  • Support continuous improvement by active participation and engagement with laboratory team for during investigations and subsequent corrective actions.
  • Ensure timely completion of all assigned documents to meet site metric requirements.
  • Participate in QC daily meetings and ensure effective communication of assigned tasks/projects etc.

Job 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.
  • Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint)
  • Proficient with Lab management software system (LIMS).
  • Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC Laboratory and ability to identify gaps in processes or systems.

If you would like to learn more about the vacancy, apply now, or contact Thaissa Torres on ttorres@elusav.com or +35315822807.

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