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Hybrid Regulatory Affairs Specialist II - On-site 4 days
Job Description & How to Apply Below
BD is a leading global medical technology company focused on urinary healthcare. The Regulatory Affairs Specialist II will lead US and CE marking submissions, support registrations in other regions, and collaborate cross-functionally to shape regulatory strategy across the product lifecycle.
This role offers on-site work four days weekly in Covington, VA, with remote Fridays. Bachelor's degree and 2+ years of regulatory affairs experience (medical devices) are required; RAC is a plus.
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