Senior Associate – QC Responsibilities Plan and perform analyses with great efficiency and accuracy. Plan and perform multiple, complex routine/ non-routine methods and procedures and a large variety of assays….

Purpose The purpose of this role is to ensure the timely and compliant release of clinical trial supplies in accordance with EU Good Manufacturing Practice (GMP) regulations. As a named…

This is a 12 month initial contract. Responsibilities QMS and maintaining it in an “Audit Ready” state. Owning CAPAs Internal quality training. Data Integrity. Change Control & Change Management process….

Qualified Person Purpose The purpose of this role is to ensure the timely and compliant release of clinical trial supplies in accordance with EU Good Manufacturing Practice (GMP) regulations. As…