Covington, Georgia
Sr. Regulatory Affairs Specialist
Job details
- Location
- Covington, Georgia
- Work type
- Hybrid
- Posted
- Aug 14, 2026
- Apply on
- bdx.wd1.myworkdayjobs.com
About this role
Bachelor of Science required and 4+ years of medical device regulatory affairs experience. Requires FDA and EU MDR knowledge, 510(k) submissions, technical files, regulatory compliance, and strong technical writing.
What you'll do at BD:
- preparing submissions
- supporting registrations
- managing compliance
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