Senior Medical Device Regulatory Lead
Insight Global
Insight Global seeks a Regulatory Specialist to support U.S. product classification, labeling, UDI/GTIN, and FDA device listings, collaborating with the Regulatory team and cross-functional partners. In a fast-paced, growth-oriented environment you will conduct regulatory impact assessments, review marketing materials for compliance, and support updates to registrations, labeling, and launches. The role covers Class I devices (with some Class II), ISO 13485, 21 CFR Part 820, GUDID, and audits, #J-18808-Ljbffr Insight Global
Vacancy posted 2 days ago
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