Medical Device Regulatory Submissions Associate

A healthcare technology company is seeking a Regulatory Affairs Associate in Arizona. The role involves preparing and submitting documentation for regulatory compliance, specifically FDA 510(k) submissions. Candidates should have a Bachelor's degree in Engineering or Biological Sciences, along with at least one year of experience in medical device regulatory and quality. Excellent communication, organizational skills, and the ability to work in a fast-paced environment are key requirements. #J-18808-Ljbffr