OverviewEinleitung Our client develops, manufactures and distributes cutting-edge surgical technology worldwide. At its location in the south of Stuttgart, we are currently recruiting for a : REGULATORY AFFAIRS MANAGER (m / f / d) Homeoffice : 50% Details : permanent position - 35 hrs. per week – 35 vacation days per yearAufgabenPreparation and updating of technical documentation for medical devices in compliance with MDR 2017 / 745Ensuring compliance with applicable regulatory requirementsDevelopment of test plans, organization of testing procedures, and definition of test characteristics and equipmentCreation of standard test reports to demonstrate compliance with relevant normsActing as the main contact for notified bodies during technical documentation reviews and regulatory inquiries from development and production teamsDefining regulatory strategies for the approval of medical devicesQualifikationA completed degree in engineering or natural sciencesProfessional experience in Regulatory Affairs for medical devicesKnowledge in the areas of ISO 13485 and MDRExcellent German (C1) and English language skills, both written and spokenStrong coordination and organizational skillsBenefitsWhat TRIGA Offers You : New career perspectives and comprehensive consulting for your personal RA careerPositions that match your skills, knowledge, and goalsExclusive job opportunities with background information about the companyOptimization of your application documents and intensive preparation for interviewsDirect access to decision-makers and negotiation of the best compensation packageNoch ein paar Worte zum SchlussYOUR CONTACT : Silvio Di Meglio Managing Director at TRIGA Consulting GmbH & Co. KG 089-8091307-21 #J-18808-Ljbffr