Hanna Syrén

I bring more than 15 years of experience from the medical device industry, combining executive leadership, quality and regulatory expertise, strategic business development, and international market implementation.
As COO and Director QA/RA I have worked across the full company lifecycle — from product development and clinical validation to regulatory approval, commercialization, and global customer implementation.

I am a hands-on and strategic leader who enjoys helping companies grow by combining structure, innovation, and clear direction. My strengths lie in navigating complex regulatory environments, driving execution, building strong collaboration across technical, clinical, and business functions, and translating technical innovation into business value.
I add the most value to growth-oriented companies within medtech, healthcare in innovation-driven industries, particularly companies facing scaling challenges, international expansion, regulatory transitions, or commercialization of advanced technologies.