Medical Device Regulatory Affairs Lead
Actalent
Actalent in Lenexa, KS, is seeking a Regulatory Affairs & Quality Compliance Specialist - Medical Devices to lead QA/RA activities and enhance the QMS across the product lifecycle. The role supports regulatory submissions, global registrations, and post-market surveillance, collaborating with cross-functional teams to ensure compliance with ISO standards and FDA QMSR. Contract to hire with onsite work in Lenexa, KS. #J-18808-Ljbffr Actalent
Vacancy posted 2 days ago
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