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QC Supervisor

  • Location: County Westmeath, Leinster, Ireland
  • Job Type:Permanent

Great opportunity for an experienced QC Supervisor to join an established and leading Pharma company in Athlone, Co. Westmeath

QC Supervisor responsibilities:

  • To supervise testing and release of In Process and Finished Products to support both commercial and development projects.

  • You will lead a group of analysts while ensuring high cGMP and GLP standards are maintained and adherence to schedules and targets to meet regulatory and business requirements.

  • Continuous management and appraisal of the performance and development of a group of analysts.

  • Perform investigations using systematic RCA approach and effective CAPA planning. 

  • Regulatory compliance through the creation and maintenance of controlled documentation for training, SOPs and analytical protocols. 

  • Preparation of documentation for audits carried out by internal auditors and Regulatory bodies. 

  • Prepare and review QC department reports and metrics e.g. monthly quality report, analysis trending reports, exceptions reports, KPI reports, etc.

  • Communicate to senior management on key events and issues etc. via normal in-house reporting structure e.g. meetings, formal reports, etc.

QC Supervisor Requirements:

  • Third level qualification (BSc or higher) in Science Related Discipline with desired 6 years’ experience in a pharmaceutical environment.

  • Previous supervisory experience.

  • Technical troubleshooting experience, understands data driven decision making, critical thinking and experienced in problem-solving skills in HPLC related methodologies, Dissolution, Moisture and Spectroscopy methodologies.

  • Excellent knowledge of laboratory testing practices, transfer and validation of analytical methods and cGMP applicable to a pharmaceutical environment.


For a confidential discussion and more information on the role, please contact Niamh Cregg.