QC Lab Specialist

Industry : Pharmaceutical

Role Description:

The QC Analyst will be responsible for coordinating and/or performing all laboratory activities including but not limited to:

  • Have an understanding and competence in GLP and laboratory workflows.
  • Perform sampling, testing, release and investigation activities associated with materials in accordance with cGMP requirements.
  • Perform analytical testing including preparation and review of documentation and any investigations for in process and finished combination products in accordance with cGMP requirements.
  • Perform analytical testing and any investigations with external test laboratories to ensure compliance to cGMP requirements.
  • Support lab support activities (Sample Management, Chemical / Consumables management, Specification / Method management, Equipment Management) to ensure compliance with local procedures and GLP requirements.

Qualification and Experience:

  • Must have minimum of Level 8 qualification in scientific discipline.
  • 2 – 3 years’ experience in Pharmaceutical QC testing Laboratory is required.
  • Experience with testing of devices / combination products / inhalation testing is preferred.


  • Demonstrated understanding of pharmaceutical QC laboratory operations and GLP.
  • Excellent communication skills must be able to comprehend and follow written and verbal procedures or instructions.
  • Must be able to work flexible schedules as required to support lab & production activity.
  • Proven ability to work cross functionally and within teams.

Duration:  Permanent role with 6 months probation.

Location:  Tipperary

To apply for this job email your details to enquiries@qaresources.com.