Regulatory Affairs Manager - Medical Devices Submissions
RAPS Institute
Collabera is seeking a Regulatory Affairs Manager for a 6+ month engagement to guide compliance with FDA and related regulations. The role involves leading regulatory submissions and ensuring alignment with ISO and other standards across diverse device projects. Required are a science/engineering degree, 5+ years in medical device regulatory affairs, and experience with 510(k) submissions. Strong communication with FDA and teams is essential. #J-18808-Ljbffr RAPS Institute
Vacancy posted more than 2 months ago
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