Covington, Georgia
Senior Manager Regulatory Affairs
Job details
- Location
- Covington, Georgia
- Work type
- Onsite
- Posted
- Aug 14, 2026
- Apply on
- bdx.wd1.myworkdayjobs.com
About this role
Bachelor's degree in a scientific or technical field; 8–10 years of medical device regulatory affairs experience, including 3–5 years in a senior or leadership role. Expertise in global submissions, FDA regulations, ISO 13485, and EU MDR.
What you'll do at BD:
- developing strategies
- submitting applications
- mentoring professionals
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