Quality Control Technician

4 weeks ago

Municipal District of Carlow, Ireland RT.Lane Full time

R.T. Lane Recruitment are currently recruiting for a Quality Control Co-Ordinator to work with a Pharmaceutical Company in Carlow.

This is an 11-month contract with strong potential for extension.

**Please note that candidates must hold the correct working visa for Ireland as my client cannot offer visa assistance and must be already residing in Ireland**

** Please note due to a high volume of applicants you will only be contacted if suitable for the position. **

Brief outline of Role:

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 MSD’s requirements to ensure compliance, safety and reliable supply to our customers.

This is a day role based onsite (Monday to Friday).

Roles and Responsibilities:

  • 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 Merck 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.
  • May be required to perform other duties as assigned.

Experience, Knowledge & Skills:

  • Proficiency in Microsoft Word, Office, Excel and job-related computer applications required i.e. LIMS.
  • Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices.
  • Understanding of Lean Six Sigma Methodology preferred but not essential.

Qualifications & Education:

  • Third Level qualification in science or related discipline.
  • GMP Experience.
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