To strengthen our team we are looking for a full-time:

Inomed Medizintechnik GmbH, headquartered in Emmendingen, is an internationally active company that develops devices and systems for the protection of nerves in order to treat patients with accurate targeting. inomed develops tools and methods in the fields of intraoperative neuromonitoring, functional neurosurgery, pain therapy and neurological diagnostics. With high-quality products and innovative technologies, the success of treatment is improved and safety is created for doctors and patients. In order to be able to optimize our applications in a targeted manner on the requirements of a dynamic market and medical everyday life, our inomed professionals work closely with users from clinic, practice and research. In this responsible position, you are significantly involved in efficiently controlling complaint processes, identifying potential for improvement and developing our quality management system. You work with interdisciplinary teams, bring your expertise into relevant standards and regulations, making a decisive contribution to maintaining the highest quality standards.

Processing of complaint processes in particular customer complaints - coordination of interdisciplinary teams and management of processes Documentation and tracking of complaints to identify trends and opportunities for improvement Support in the care, maintenance and optimization of our internationally oriented QM system, including ISO 13485, 21 CFR 820, MDR (Regulation 2017/745) and MDSAP Planning, implementation and support of internal, external and supplier audits Coordination and cooperation at CAPA and supplier management Support and active participation in the implementation of process changes and optimizations Coordination and monitoring of all QM relevant training by CAQ software (e.g. e-learning) Support for the various business areas of QM relevant topics

Complete vocational training or studies in the field of quality management, medical technology or comparable qualifications Technical understanding and independent, targeted and systematic work and action Ideally knowledge of the essential standards and regulations of medical technology, in particular ISO 13485, 21 CFR Part 820, 2017/745 (MDR), MDSAP Knowledge of complaint and CAPA management Very good English skills in word and writing High reliability and quality awareness Solution-oriented, efficient and responsible approach with high quality awareness

We offer you cooperation in a growing medical technology company with colleagues from all over the world We grant your company pensions We support the reconciliation of family and work through sliding time and mobile work We promote talent through individual training opportunities We subsidize your daily breakfast or lunch in our restaurant In addition to the attractive remuneration, you will be given the opportunity for a variety of other benefits such as Hansefit, Jobrad, Corporate Benefits and many more. You work in a modern company seat with high-quality technical equipment You become part of a team with flat hierarchies and a company-wide duz culture JOBV1_EN