Quality & Regulatory Affairs Specialist: CAPA & Compliance
VERO Biotech
VERO Biotech in Atlanta, GA, seeks a Quality Compliance Specialist to support QMS administration across training, investigations, nonconformance, CAPA, deviations, change control and internal audits. You will help ensure timely investigations with root-cause analysis and risk evaluation in line with VERO procedures. You will work closely with the Director of Quality Compliance to maintain robust documentation and KPI trending, driving continuous improvement while adhering to FDA and ISO #J-18808-Ljbffr VERO Biotech
Vacancy posted 2 days ago
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