
QC Validation Specialist
- Ireland
- Permanent
- Full-time
- Help develop and validate new and existing test methods for gene therapy products.
- Create and analyse protocols, reports, and data to support method transfer activities.
- Ensure all methods meet regulatory standards and maintain data integrity.
- Write and update standard operating procedures (SOPs) for validated methods.
- Communicate progress and updates on method transfers to stakeholders.
- Regularly review analytical methods to ensure they are functioning as expected.
- Support the maintenance of the Quality Management System and document control processes.
- Track and achieve personal goals and timelines effectively.
- Perform testing of gene therapy products when required, ensuring alignment with production schedules.
- Background in human health or sciences, with relevant qualifications.
- Experience in quality control or analytical method validation in a regulated industry.
- Familiarity with techniques such as qPCR, HPLC, ELISA, Western blot, cell culture, and DNA extraction.
- Knowledge of ICH Q2 R1 guidelines and proficiency in Microsoft Office tools.
- Strong organizational and communication skills.
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