Regulatory Affairs Specialist — MedTech Submissions

Becton Dickinson in Covington, GA is seeking a Regulatory Affairs Specialist I to support regulatory strategies and submissions for medical devices across the product lifecycle, collaborating on domestic and international registrations.

The role emphasizes preparing 510(k) s, IDEs, and PMAs, maintaining regulatory documentation, and ensuring labeling compliance while communicating with FDA and regulators worldwide to keep products on schedule.

For the Regulatory Affairs Specialist I — Med Tech Submissions position at Becton Dickinson, we are reviewing applications now.

Consider building your career as a Regulatory Affairs Specialist I — Med Tech Submissions at Becton Dickinson.

The Regulatory Affairs Specialist I — Med Tech Submissions position in the Legal, Management & Operations field is open for applications.

We have an opening for a Regulatory Affairs Specialist I — Med Tech Submissions in Covington, GA, United States within Legal, Management & Operations.