Regulatory Affairs Specialist

BD

Tempe, AZ, United States
Fully remote
Prepare regulatory submissions
Global markets
Product lifecycle support
The RA Specialist prepares regulatory submissions required to market new or modified medical devices in global markets

Job Summary

  • The RA Specialist prepares regulatory submissions required to market new or modified medical devices in global markets.
  • The RA Specialist may participate independently on new product development teams and provide continued RA support through the lifecycle of the product.
  • BD is one of the largest global medical technology companies in the world, advancing the world of health.

Matching Summary

The RA Specialist prepares regulatory submissions required to market new or modified medical devices in global markets.

Skills & Requirements

Must-have

  • prepare regulatory submissions
  • global markets
  • product lifecycle support
  • interpret regulatory issues
  • quality system principles

Nice-to-have

  • detail-oriented and methodical
  • work with minimal supervision
  • team-oriented environment
  • fast-paced environment

Key Requirements

  • Bachelor's degree or advanced degree in technical area
  • Minimum of one year of experience
  • Previous experience in medical device industry
  • Previous experience in Regulatory Affairs
  • Ability to travel up to 25%

Work Rights

Not specified

Tailored Resume

Cover Letter