Laura Vanonen is a quality assurance and regulatory affairs professional in the medical device industry, currently serving as the QA&RA Manager at MEGIN. They hold a Master of Science in Materials Science and Engineering and have extensive experience in product quality, regulatory compliance, and environmental standards. Previously, Laura worked as a Complaint Coordinator at KaVo Kerr Group and served as a Regulatory Specialist focused on product environmental compliance. Their expertise encompasses FDA regulations, ISO standards, and medical device compliance.
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