Regulatory & Clinical Affairs Manager (FDA 503B)
QuVa Pharma
QuVa Pharma seeks a Manager of Regulatory & Clinical Affairs to ensure regulatory compliance and labeling accuracy across all sites. You will coordinate third party submissions, oversee CSP/bulk artwork, evaluate finished drug products for label compatibility, and support FDA inspections related to labeling within the FDA 503B framework. You will lead cross-functional teams, manage investigations and CAPAs, and drive continuous improvements while aligning regulatory activities with business #J-18808-Ljbffr QuVa Pharma
Vacancy posted 4 days ago
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