Appply here (!): https://positrigo-ag.breezy.hr/p/73946325f971-medical-device-regulatory-affairs-and-quality-affairs-ra-qa-manager We are looking for a broad RA/QA Manager who will navigate the processes and drive the documentation development of our medical device NeuroLF. You will be responsible for developing and implementing quality and regulatory functions at our company. You help drive the development by contributing to our technical documentation such as user inputs, usability, and systematic risk assessments. You will get firsthand RA/QA support by external experts in the field. You will coordinate our internal and external collaborators. You help build complex medical products while ensuring high quality, reliability, safety for patients, and maintainability.