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
How To Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to [email protected] and tell me why you’re interested. Or, feel free to email your resume. Please include Job#20006.