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A seasoned Quality Assurance and Regulatory Affairs professional with 20+ years of experience in pre-market and post-market product development of life science & biotech products and medical devices, including medical device vigilance and post-market surveillance. Hands-on experience in establishing Quality Systems supporting pre-clinical and clinical product development and product release to market. Marion earned her PhD in Molecular Biology at the University of Zurich and an MBA from Webster University, Geneva.