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Job description
Quva seeks a Manager of Regulatory & Clinical Affairs to ensure labeling accuracy and regulatory compliance across all sites. You will oversee third party submissions, support CSP and bulk artwork development, and align activities with FDA 503B requirements to protect patient safety and product quality.
You will lead investigations, assist with customer onboarding via ASHP assessments, and partner with cross-functional teams to drive continuous improvement and operational excellence in a
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Worksite address
sugar land, TX, 77479, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.