I started my career in the field of Medical Devices at SP-Medical, where I bring experience in quality and regulatory tasks. SP Medical has exposed me to various areas, including Risk Management, validation, bioburden, and technical documentation.I have completed the following courses in Medical Devices:ISO 13485 and Quality Management for Medical Devices / Internal AuditingMedical Device Usability & IEC 62366-1 and -2Risk ManagementBioburdenPackaging validationInternal Auditing & ISO 19011I believe in a solution-oriented approach, based on Aaron Antonovsky's concept of coherence. By focusing on predictability, stress balance, and involvement, we can achieve comprehensibility, manageability, and meaningfulness, forming the foundation for effective collaboration towards a common goal.I work in an analytical and reflective manner, and I am motivated by promoting quality, development, and optimization. I find motivation in the opportunity to tackle tasks where I am both part of a process and able to deliver results. Additionally, I thrive in cross-functional teamwork and collaboration with external partners.Feel free to connect with me on LinkedIn!