Medical Device Regulatory Affairs Rotations Program

Abbott currently offers several opportunities for the Medical Device Regulatory Affairs Development (RAD) Program, located in Alameda, Pleasanton, Santa Clara, CA, Minneapolis, MN or Plano, TX. The role entails three 1-year rotations, with regulatory documentation preparation, submissions, and global regulatory operations tasks.

You'll work to ensure compliance with FDA and worldwide regulations, while supporting product releases and regulatory strategies across multiple sites and teams.