At Advanced Accelerator Applications, a Novartis company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy to cancer patients. We are looking for an experienced Compliance Specialist with previous experience in a GMP Biopharmaceutical environment to help us reach our ambitious goals.

As a Compliance Specialist, you will be responsible for implementing robust Quality Systems at our new Radioligand Therapy (RLT) Isotope Manufacturing site in Indianapolis incorporating Novartis and regulatory requirements. You will contribute significantly to the execution of these systems, author or contribute to the procedures governing these systems and work towards timely implementation. You will participate in Quality Management Reviews, Self-Inspections, trainings and in health authority inspections.