GMP QC Specialist for Gene Therapy Analytics

A leading biotech firm in Ireland is seeking a QC Specialist responsible for ensuring compliance with Good Manufacturing Practices within QC to support gene therapy products. The ideal candidate should possess at least 8 years of experience in the pharmaceutical industry and a degree in Human Health or Sciences. Responsibilities include managing QC activities, supporting technical transfers, and ensuring timely resolutions of QC issues as well as maintaining documentation compliance.