Ensuring structured, controlled and compliant technical documentation within the quality management system - You are a strong match if you combine solid experience in regulatory affairs and quality management with a pragmatic, solution-oriented mindset and the ability to drive cross-functional collaboration in complex environments. * 5+ years of professional experience in medical devices or IVD, with exposure to Regulatory Affairs and Quality Management * Excellent stakeholder management and communication skills in international environments - Working in an innovative and international environmentwith a broad learning and development landscape in our EMEA Campus, after-work events for internal networking - Subsidized EGYM Wellpass with access to 13,500 studios, plus in-house gym, various sports courses, massages, company medical and psychological care, workplace glasses, and general ...
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