To strengthen our team we are looking for a full-time: Projektmanager (m/w/d) 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. As a team member in Regulatory Affairs, you work with a focus on care and implementation of national and international approvals of our medical devices. Together with the responsible areas, You develop strategic orientations and market strategies. You expect the following exciting tasks:

Implementation and support for national / international new and repetition authorisations Developing and implementing authorisation strategies in the fields of product management, development and sales Participation in the preparation of country-specific admission documents Research into regulatory requirements and implementation in the company Self-employed communication with the respective national authorities, traders and service partners Participation in development projects as a specialist for admission issues Support for the maintenance, maintenance and optimization of the QM system according to ISO 13485, 21 CFR 820, MDSAP, MDR (2017/745), Taiwan, South Korea and, where appropriate, other countries

Complete training or studies in Regulatory Affairs, Medical Technology or equivalent qualification in a scientific field Professional experience in the field of national/international admissions in medical technology Knowledge of the essential norms and regulations of all MDSAP member states and the European Regulation 2017/745 (MDR) Good knowledge in one or more fields: medicine, electronics, mechanics and materials sciences Very good English skills in word and writing Good MS Office and ERP knowledge, ideally Microsoft Dynamics 365 BC (NAV) High reliability and high quality awareness Self-employed work by appointment and safe occurrence

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