HTI is hiring In-Process Quality Assurance Auditors for PAI in Greenville, SC. These are Direct Hire, Full-Time, 12-Hour Shifts positions with starting at $25, plus $1.25/hour shift differential for night shifts. EXCELLENT, comprehensive benefits package provided. Work in a climate-controlled pharmaceutical manufacturing environment within a regulated facility.
Job Summary – In-Process Quality Assurance AuditorEnsures 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
INDPRO