Support Nonconformance Event (NCE) and CAPA processes
Ensure accurate, timely, and compliant documentation
Identify, document, and escalate quality risks
Support internal audits, regulatory inspections, and quality assessments
Collaborate with QA leadership and cross-functional partners
Complete all required training in accordance with established timelines
Perform other duties as assigned to support quality and business objectives
Requirements
Associate degree or equivalent experience
Certified Quality Professional (CQE, CQA, etc.) a plus
Lean Six Sigma (or other Continuous Improvement) certification a plus
Minimum of 1-3 years of related experience with exposure to quality, supply chain management (distribution) and/or pharmaceuticals or combination of equivalent education and experience.
Strong technical writing skills
Working knowledge of Drug Supply Chain Security Act (DSCSA)
Demonstrated ethical conduct
Strong verbal and written communication skills
Strong organizational skills and attention to detail
Proficiency in Microsoft Office applications (Excel, Word, PowerPoint)