Position Title: Quality Assurance Auditor

Location: Greenville, South Carolina

Job Summary – In-Process Quality Assurance Auditor
Ensures consistent product quality through independent in-process inspection, testing, verification, and auditing of pharmaceutical products during manufacturing and packaging operations in a cGMP-regulated environment. This role supports real-time compliance, documentation accuracy, and quality decision-making on the production floor.What We Offer

• Full benefits package – Medical, Dental, Vision, EAP, 401(k) with company match
• 12HR day and 12HR night shifts available
• Night shift differential ($1.25/hour)
• Paid Time Off and company holidays
• Stable, direct-hire role in a regulated pharmaceutical environment
• Climate-controlled manufacturing facility
• Nicotine-free campus supporting employee wellness

What You Need

• High School Diploma or GED required (Associate degree preferred)
• Minimum 2 years of QA or QC experience in a regulated manufacturing environment
• Strong understanding of cGMP and FDA regulations
• Experience reviewing batch records and GMP documentation
• Ability to work independently with minimal supervision
• Strong attention to detail and documentation discipline
• Ability to manage shifting priorities in a fast-paced manufacturing environment
• Willingness to work 12-hour shifts and travel between nearby buildings during shift

Responsibilities –

• Perform in-process inspections and audits during manufacturing and packaging operations
• Verify executed documentation for accuracy, completeness, and data integrity
• Conduct in-process testing (pH, specific gravity, sampling, compounding calculations)
• Identify, document, and escalate non-conformances and deviations
• Initiate events in TrackWise and support investigations and CAPAs
• Perform line and room clearance inspections prior to production start
• Verify labeling, serialization/aggregation (DSCSA), and component reconciliation
• Collaborate with Manufacturing, Packaging, and Quality teams to resolve quality issues
• Support SOPs, work instructions, and continuous improvement initiatives
• Follow all company policies, procedures, and applicable regulatory requirements

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