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Rachel Kent
Life Science

+353 87 427 8808
[email protected]
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Details

QC External Sample and Retain Coordinator


Reference:RK22735 Location: Carlow
Qualification:DegreeExperience:2-3 Years
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: QC Analyst

QC External Sample and Retain Coordinator
RK22735
Contract – 11 months
Carlow


We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Carlow. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.


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, consistent with requirements to ensure Compliance, safety and reliable supply to our customers. This is a Day role based on site (Mon-Fri)


Duties:

• Will act as point of contact for QC sample and retain management.
• Responsible for QC External sample management from receipt to shipment.
• Responsible for QC retain sample management from receipt to disposal.
• Knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC Laboratory and ability to identify gaps in processes or systems.
• Proficient with using Microsoft Office applications (Outlook, Excel, Word, and PowerPoint).
• Proficient with Lab management software system (LIMS).
• Prepare documents and coordinate Sample movement within the Warehouse area.
• Review eLogs and/ or LIMs to align physical quantities of samples in freezers/refrigerators/lean lifts and sample cages.
• 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 Global Policies, Procedures and Guidelines, regulatory requirements.
• Support continuous improvement by active participation and engagement with laboratory team during investigations and subsequent corrective actions.
• Ensure timely completion of all assigned documents to meet site metric requirements.
• Work collaboratively to drive a safe and compliant culture in Carlow.
• Participate in QC daily tier meetings and ensure effective communication of assigned tasks/projects.


Experience and Education:

• Bachelor’s Degree or higher preferred; ideally in a science related discipline.
• 2+ years’ GMP experience, ideally in Quality within the Biological and/or pharmaceutical industry.
• Quality Control experience preferable


If interested in this posting please feel free to contact Rachel Kent at Life Science Recruitment for further information.