Job description: In this role, you will be responsible for ensuring compliance with regulatory requirements for drug approval. You will be part of the Regulatory Affairs team and work closely with other departments to ensure that all required documents and data are submitted on time. They also support the development of strategies for the successful approval of medicines.

Job Description: In this role you will be responsible for developing, implementing and maintaining qualification and validation plans as part of the quality management system. You are the contact person for internal and external customers for questions about qualification and validation and also carry out training.

Job description: In this role you are responsible for coordinating the European approval of medical devices. You are the contact person for internal and external customers for questions regarding the European approval of medical devices and also carry out training courses. You will work closely with other departments to ensure timely submission of admission applications.

Job Description: In this role you will be responsible for developing, implementing and maintaining risk management plans within the quality management system. You are the contact person for internal and external customers with questions about risk management and also carry out training courses.

Job Description: In this role you will be responsible for developing, implementing and maintaining CAPA systems as part of the quality management system. You are the contact person for internal and external customers with questions about the CAPA system and also carry out training courses. You will work closely with other departments to ensure that CAPA measures are implemented appropriately and in a timely manner.