In Process Quality Assurance Auditor - (12 Hr Night 7p-7a)

About the role

The In Process Quality Assurance Auditor ensures consistent product quality through independent inspection in process testing, verification and auditing of pharmaceutical drugs during manufacturing and packaging within a cGMP-regulated pharmaceutical manufacturing environment. This position provides intermediate-level Quality Assurance support across manufacturing, warehousing and packaging operations. The In Process Quality Assurance Auditor applies critical thinking, analytical reasoning, and sound judgment to evaluate data, identify deviations, and ensure compliance with internal procedures and regulatory requirements (FDA, DEA).

Responsibilities

• Promote and ensure compliance with current Good Manufacturing Practices (cGMPs) and all applicable regulatory standards.
• Independently perform in-process inspections throughout manufacturing and packaging operations to verify conformance to specifications.
• Conduct verification of production operations and environmental conditions prior to line clearance and batch initiation.
• Perform in-process testing (pH, specific gravity, etc.) and assay calculations for compounding operations.
• Review batch records, logbooks, and associated documentation for completeness and compliance as the process is in production; verify data accuracy and documentation integrity.
• Identify out of trends or non conformances from documented data or auditing on the line from in process testing results, review of label print and application, DSCSA serialization/aggregation, downtime activities, and proactively communicate to put in corrective actions prior to the product being removed from the area.
• Record inspection results and maintain accurate data in quality systems (SAP, WMS, and other databases).
• Identify, segregate, and document non-conforming events on the process line, and halt the processing if critical compliance activities are identified (e.g., product spills, equipment set up incorrectly, label print incorrect, mixed components on the line).
• Immediately escalate non conformance or observations to management for direction.
• Initiate non conformances in TrackWise system and assist in investigations.
• Apply critical thinking to evaluate quality data, assess deviations, and determine appropriate actions or escalation.
• Support Process Issues (PIs) and Corrective and Preventive Actions (CAPAs) by providing detailed, factual information.
• Collaborate with manufacturing and packaging personnel to resolve quality issues and ensure adherence to quality standards.
• Participate in continuous improvement activities to enhance product quality and operational efficiency.
• Conduct packaging room and line clearance inspections prior to production start-up.
• Verify reconciliation of components after batch completion and ensure proper documentation and return to inventory