Megha Kanth is a quality assurance professional with over 7 years of experience in the pharmaceutical and medical device industries. Currently serving as the APAC Lead for Quality Assurance at Cytiva, they specialize in ISO 13485, FDA, and cGMP compliance. Megha has a strong record of enhancing operational efficiency, including increasing team efficiency by 95% through training at Prewel Labs. They hold a Bachelor’s degree in Biotechnology from Thiruvalluvar University and a Master’s degree from Bangalore University. Megha is passionate about driving quality improvements and is seeking new opportunities to leverage their leadership and regulatory expertise.
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