In-Process QA Auditor — Pharma Compliance & Verification

PAI Pharma; Greenville (SC); On-site; USD 70,000 - 90,000; Full time

Job summary

PAI Pharma is seeking an In Process Quality Assurance Auditor to ensure product quality through in-process testing, inspections, and auditing within a cGMP-regulated pharmaceutical manufacturing environment. This role supports manufacturing, warehousing and packaging operations, applying critical thinking to evaluate data, identify deviations, and ensure FDA/DEA compliance.

Responsibilities include performing inspections, reviewing batch records, initiating non-conformances in TrackWise, and

Qualifications

• Requires a high school diploma or GED; associate degree preferred.
• Minimum 2 years of QA/QC experience in a pharmaceutical or regulated manufacturing environment.

Responsibilities

• Promote and ensure cGMP compliance and regulatory standards.
• Independently perform in-process inspections to verify conformance to specifications.
• Review batch records and documentation for completeness and compliance; identify non-conformances.
• Initiate non-conformances in TrackWise and assist in investigations; support CAPAs.

Skills

Critical thinking

Attention to detail

Communication

Prioritization

Interpersonal

Math aptitude

Self-motivation

Education

High school diploma or GED

Associate degree preferred

Tools

Microsoft Office

SAP/WMS

Job description

PAI Pharma is seeking an In Process Quality Assurance Auditor to ensure product quality through in-process testing, inspections, and auditing within a cGMP-regulated pharmaceutical manufacturing environment. This role supports manufacturing, warehousing and packaging operations, applying critical thinking to evaluate data, identify deviations, and ensure FDA/DEA compliance.

Responsibilities include performing inspections, reviewing batch records, initiating non-conformances in TrackWise, and