Mahima Gupta has a diverse work history in the field of regulatory affairs and compliance. Mahima most recently worked as a Regulatory Affairs & Compliance Specialist at Yukon Medical, LLC starting in 2022. Prior to that, they worked at Freyr Inc. as a Regulatory Affairs Analyst from 2018 to 2022. In this role, they managed US FDA communications for various applications and assisted foreign pharmaceutical companies with site/facility registration. Mahima also gained experience as a Regulatory Intern at John Hopkins Bloomberg School of Public Health in 2018, where they conducted research and compared regulations for in-vitro tests across different regulatory agencies. In 2017, they worked as a Regulatory Intern at Synaptive Medical and successfully developed a strategy for registering medical devices in several international jurisdictions. Their first internship in 2015 was at Azine Healthcare Pvt Ltd, where they gained experience in quality control and process documentation for pharmaceutical manufacturing.
Mahima Gupta's education history includes a Bachelor of Pharmacy (BPharm) degree from Nirma University in Ahmedabad, Gujarat, India, which they completed between 2012 and 2016. Following this, they pursued a Master of Science (MS) degree in Regulatory Affairs from Northeastern University from 2016 to 2018. Lastly, they obtained a Master of Business Administration (MBA) degree from the University of the Cumberlands, where they studied from 2019 to 2022. The field of study for their MBA and BPharm degrees is not specified.
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