As Quality Manager (m/f/d) you will ensure that we work in harmony with legal regulations and guidelines. You will work very closely with the other departments to establish and further develop an appropriate quality assurance system with elements such as deviations and change procedures.
Your knowledge of the European regulations of Good Manufacturing Practice, drug manufacturing, and cell and gene therapies, makes you a competent contact person for quality assurance issues. Thus, you will actively contribute to ensuring that the batches we produce are safe, effective, and of good quality, so that they can be used for the therapy of seriously ill patients. In this context, your tasks will also include the monitoring and follow-up of audits, as well as the qualification of materials and suppliers, and the creation and management of quality assurance agreements. Our Quality Managers are particularly characterized by a sense of responsibility, initiative, and excellent communication skills.