Regulatory Affairs Manager

BD

Covington, GA, USA
Fully remote
Lead and manage regulatory submissions
Medical device regulatory requirements
Prepare and submit regulatory filings
The Regulatory Affairs Manager will lead and manage regulatory submissions, approvals, and compliance activities for medical devices

Job Summary

  • The Regulatory Affairs Manager will lead and manage regulatory submissions, approvals, and compliance activities for medical devices.
  • This role ensures that products meet all national and international regulatory requirements, facilitating timely market access and maintaining post-market compliance.
  • BD is one of the largest global medical technology companies in the world, advancing the world of health.

Matching Summary

The Regulatory Affairs Manager will lead and manage regulatory submissions, approvals, and compliance activities for medical devices.

Skills & Requirements

Must-have

  • lead and manage regulatory submissions
  • medical device regulatory requirements
  • prepare and submit regulatory filings
  • liaison with regulatory agencies
  • interpret complex regulatory requirements
  • conduct regulatory assessments

Nice-to-have

  • advancing the world of health
  • imagination and passion
  • human element across global teams
  • learn grow and become your best self

Key Requirements

  • Bachelor's degree in scientific, engineering, or related field
  • Minimum of 5-7 years of experience in Regulatory Affairs
  • Experience in the medical device industry
  • Ability to work on-site in Covington, GA
  • RAC (Regulatory Affairs Certification) preferred

Work Rights

Not specified

Tailored Resume

Cover Letter