BD
Covington, Georgia

Sr. Regulatory Affairs Specialist

HybridPosted 3 weeks ago

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Job details

Location
Covington, Georgia
Work type
Hybrid
Posted
3 weeks ago
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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About BD

BD
Covington, Georgia