Quality Control (QC) Associate

The Quality Control (QC) Associate plays a key role in maintaining the integrity of materials, manufacturing inputs, and final product quality across the GMP site. Supporting the Quality Assurance leadership, the QC Associate is responsible for conducting material checks, coordinating lab testing, managing documentation, and contributing to quality investigations. This role supports the overall Pharmaceutical Quality System and helps ensure compliance with EU GMP, pharmacopeial standards, and applicable Jersey medicines regulations. It is ideally suited to a detail-oriented individual with hands-on experience in a GMP or compounding environment.