Quality Assurance Auditor

Quality

Greenville, South Carolina

Professional Direct Hire

Sep 18, 2026

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 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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