Andreia Domingues is a Senior Regulatory Affairs Specialist with 11 years’ experience navigating medical device regulation across EMEA, MDSAP and Asian markets, currently at Cytiva. She blends a biomedical and pharmaceutical medicine background with hands-on regulatory operations—technical files, STED, CERs, MDR gap analysis and global license renewals—to move products from development to compliant market access. Formerly a bench neurobiologist turned RNA biology and data enthusiast, she combines lab fluency with regulatory strategy and data-driven mindset. Andreia has led cross-functional projects, trained newcomers, and prepared for external/internal audits, showing strength in both detail-oriented documentation and stakeholder communication. Based in Montreux, she brings practical experience with ISO 14971 risk management and international registrations, plus an uncommon mix of childcare leadership roles that sharpened her planning and empathy.
11 years of coding experience
Bachelor's degree, Biomedical Sciences, Bachelor's degree, Biomedical Sciences at University of Aveiro
Contributions:16 commits, 7 pushes, 1 branch in 1 year 4 months
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Andreia Domingues - Senior Regulatory Affairs Specialist I