Now Hiring: In-Process Quality Assurance Auditor (3x12 Shift | 7 AM – 7 PM)
📍 Greenville, SC | Full-Time
We’re looking for a detail-oriented and analytical In-Process Quality Assurance Auditor to join our team in a fast-paced, cGMP-regulated pharmaceutical manufacturing environment. This role is critical in ensuring product quality, compliance, and operational excellence across manufacturing and packaging processes.
What You’ll Do:
- Perform in-process inspections and testing to ensure product quality and compliance
- Verify production readiness, line clearance, and environmental conditions
- Review batch records and documentation for accuracy and regulatory compliance
- Identify and escalate non-conformances; support investigations and CAPAs
- Collaborate with cross-functional teams to resolve quality issues
- Maintain accurate records in quality systems (SAP, WMS, etc.)
- Support audits, SOP updates, and continuous improvement initiatives
What We’re Looking For:
- 2+ years of QA/QC experience in pharmaceutical or regulated manufacturing
- Strong knowledge of cGMP, FDA, and DEA regulations
- Experience with batch record review, in-process testing, and quality systems
- Excellent attention to detail, analytical thinking, and problem-solving skills
- Proficiency in Microsoft Office; SAP/ERP experience is a plus
Why Join Us?
You’ll play a key role in safeguarding product quality while working in a collaborative, compliance-driven environment that values precision, accountability, and continuous improvement.
