Karan Modi, Ms Ra, Rac
About Karan Modi, Ms Ra, Rac
Karan Modi is the Regulatory Affairs Team Lead at Teleflex Incorporated in Morrisville, with over a decade of experience in regulatory affairs and quality assurance across the pharmaceutical and medical device industries.
Company
Karan Modi is currently employed at Teleflex Incorporated in Morrisville. Teleflex is a global provider of medical technologies designed to improve the health and quality of people’s lives. Karan joined Teleflex in January 2019 and is currently serving as the Regulatory Affairs Team Lead, bringing his extensive experience in regulatory affairs and quality assurance to the company.
Title
Karan Modi holds the position of Regulatory Affairs Team Lead at Teleflex Incorporated. In this role, he leads the regulatory affairs team, ensuring compliance with regulations, managing submissions to health authorities, and overseeing the development and execution of regulatory strategies for medical devices.
Education and Expertise
Karan Modi obtained a Master of Science (MS) degree in Drug Regulatory Affairs from Long Island University, Brooklyn Campus, where he studied from 2009 to 2011. Prior to this, he earned a Bachelor of Science (BS) degree in Pharmacy from Rajiv Gandhi University of Health Sciences, studying from 2004 to 2008. His educational background has equipped him with in-depth knowledge of drug regulatory processes, pharmaceuticals, and medical devices.
Background
Karan Modi has accumulated over a decade of experience in regulatory affairs and quality assurance, having worked in various roles across multiple industries including pharmaceuticals and medical devices. His professional journey has taken him through different geographies and positions, ranging from intern to team lead. He has worked for companies like Stryker, Air Techniques, and Pharbest Pharmaceuticals, in addition to an academic stint at Long Island University.
Career Path and Experience
Karan began his career as an intern at RPG Life Sciences in India in 2008. He then progressed to a Quality Assurance Associate role at RPG Life Sciences Limited for 6 months in 2009. Moving to the United States, he served as a Regulatory Affairs/Quality Assurance Officer at Pharbest Pharmaceuticals from 2011 to 2014. He also held the position of Quality Systems and Regulatory Affairs Associate at Air Techniques in Melville, NY, from 2014 to 2015 followed by a significant role as Senior Regulatory Affairs Specialist at Stryker in Kalamazoo, MI, from 2016 to 2019. His diverse experiences have shaped him into a versatile expert in the field.