Regulatory Affairs Intern

Summary

Join Lexington Medical's Summer Intern Program to contribute to the progress of the company and gain business acumen and real-world experience.

Requirements

Must be a rising junior or above attending an accredited university majoring in Regulatory Affairs, Biomedical Engineering, or similar

Responsibilities

• Participate in the development and implementation of regulatory strategies for new and existing products
• Prepare global product registrations
• Support the maintenance of regulatory files and documentation to ensure compliance
• Support regulatory efforts required to align with new regulations (e.g., EU MDR, MDSAP) and requirements including changes to international standards
• Review product labeling, promotional materials, and advertising materials to ensure regulatory compliance
• Represent Regulatory Affairs on cross-functional product development and manufacturing engineering teams. Guide teams to provide content for US and/or international submissions; participate in design reviews as needed