Global Regulatory Affairs Lead - Medical Devices
Remote Jobs
Medline Industries, LP seeks a Senior Regulatory Specialist to plan and execute global regulatory projects for device approvals, including strategies for new markets and post-market changes. You will lead multifunctional teams and ensure content quality for regulatory submissions. Required are a BA/BS in life sciences or related field and at least 4 years in regulatory affairs for medical devices, with experience on 510(k) and CE submissions. Travel up to 10% is expected. #J-18808-Ljbffr
Vacancy posted 4 days ago
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