Senior Regulatory Affairs Specialist

BD

Covington, GA, United States
Fully remote
Regulatory strategy development
Cross-functional teamwork
Medical device submissions
The Senior Regulatory Affairs Specialist will work on regulatory strategy and submissions for urinary devices

Job Summary

  • The Senior Regulatory Affairs Specialist will work on regulatory strategy and submissions for urinary devices.
  • The role involves leading cross-functional teams in preparing and implementing submissions to the US FDA and European Notified Bodies.
  • BD values collaboration and supports employees in their growth and development.

Matching Summary

The Senior Regulatory Affairs Specialist will work on regulatory strategy and submissions for urinary devices.

Skills & Requirements

Must-have

  • regulatory strategy development
  • cross-functional teamwork
  • medical device submissions

Nice-to-have

  • strong communication skills
  • self-motivated individual
  • global perspective

Key Requirements

  • Bachelor of Science required
  • minimum 5 years experience in Regulatory or Quality
  • knowledge of US and European medical device regulations

Work Rights

Not specified

Tailored Resume

Cover Letter