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 - 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 health management Various opportunities to get involved in different sustainability and charity initiatives, climate friendly and respectful use of resources
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