LEO Pharma Cork are currently recruiting a Quality Specialist to join our team. This is a contract position, reporting to the Senior Manager, Quality, Operations Cork, and will have responsibility for cGMP compliance support of API manufacturing.
Responsibilities
- Supporting the full range of daily compliance activities on the Cork site.
- Day to day compliance activities including: raw material and intermediate release, approval of Change Control, Deviations, Change Actions and CAPA, and supporting the QC Laboratories, Maintenance and Operations departments.
- Collaboration with other functions both globally and locally on Quality Improvement Initiatives.
- Review and approval of Standard Operating Procedures, Test Methods and Protocols.
- Participating in timely execution of KPI for the Quality department.
- Participating in continuing professional development to maintain awareness in current and new regulations and ensuring new regulations are implemented.