Regulatory Affairs Specialist
Regulatory Affairs Specialist with experience in quality assurance, technical writing, and compliance for medical devices. He holds a master’s degree in materials engineering and a postgraduate qualification in quality management from AGH University of Krakow.
His background includes working with MDR requirements, audits, and documentation in regulated environments. On a daily basis, he supports projects by ensuring alignment with regulations and standards, while also contributing to the quality and accuracy of blog content.
