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.
*FULL SPEC ON APPLICATION**
For a confidential discussion and more information on the role, please contact Niamh Cregg.