Job Title: QC External Sample and Retain Coordinator
We are currently recruiting for an exciting opportunity with a leading multinational pharmaceutical organization. This position is ideal for individuals seeking to join a top-performing company in the industry.
Responsibilities:
* Act as point of contact for QC sample and retain management.
* Manage QC external samples from receipt to shipment, ensuring timely and accurate delivery.
* Manage QC retain samples from receipt to disposal, adhering to current Good Manufacturing Practices (cGMP).
* Understand cGMP related to the QC Laboratory and identify gaps in processes or systems.
* Proficiently use Microsoft Office applications (Outlook, Excel, Word, PowerPoint) and 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.
* Oversee processes related to sample handling, including freezer/refrigerator clean schedules.
* Support sample management-related non-conformance investigations.
* Support Internal and Regulatory Audits.
* Format, write, and deliver necessary documentation in line with Global Policies, Procedures, and Guidelines, regulatory requirements.
* Support continuous improvement by engaging with the laboratory team during investigations and 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.
Requirements:
* Bachelor's Degree or higher, preferably in a science-related discipline.
* At least 2 years' GMP experience, ideally in Quality within the Biological and/or Pharmaceutical industry.
* Quality Control experience is preferable.