Description
Cellares is seeking a Senior Director of IDMO Site Quality to lead the Quality organization (QA/QC) and oversee cGMP Operations within a cell therapy manufacturing facility. This role involves providing strategic leadership, ensuring regulatory compliance, and driving effective communication across cross-functional groups to produce and release cell therapy products to patients. The candidate should have extensive experience in Quality Management within a cGMP environment, preferably with cell/gene therapy and CDMO experience, and possess strong leadership, analytical, and communication skills.
