Director Quality

Director, Quality Assurance Location: Greater Greenville, SC Area Some relocation support offered Lead enterprise-wide quality operations for my client in a highly regulated cGMP manufacturing environment. This is a high-impact leadership role driving compliance, continuous improvement, and product quality while building a culture of excellence. Why You Should Apply Lead Quality Assurance, QC Inspection, and Document Control Influence company-wide quality strategy and compliance Drive modernization of electronic Quality Management Systems Build and mentor a high-performing quality team What You’ll Be Doing Lead QA/QC operations, document control, CAPA, deviations, audits, and change control Oversee material and finished goods release and batch certification Ensure compliance with cGMP, FDA, OSHA, and regulatory requirements Direct internal/external audits, supplier quality, investigations, and training Champion continuous improvement and cross-functional quality initiatives About You Bachelor's degree in a related field Experience leading QA within a cGMP manufacturing environment Strong knowledge of CAPA, change control, document control, audits, and quality systems Proven leadership, coaching, and talent development skills Excellent problem-solving, regulatory, and cross-functional communication abilities #J-18808-Ljbffr Scientific Search