Med Device Regulatory Affairs Specialist - Hybrid
Actalent
Actalent in Fort Worth, TX, seeks a Regulatory Affairs Specialist to prepare and submit regulatory documents for medical devices, ensuring compliance with FDA QMSR, 21 CFR Part 820, and EU MDR. The role supports audits, CAPA, PMS, CER, and PMCF activities while guiding regulatory strategies for global products. You will collaborate with Manufacturing, Product Development, Marketing, and Sales to ensure compliant processes and product claims, and stay ahead of evolving regulatory requirements in #J-18808-Ljbffr Actalent
Vacancy posted 4 days ago
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