Quality Auditor

Quality Auditor About the Opportunity

We are hiring two Quality Auditors for an onsite contract opportunity with a manufacturing organization in Memphis, TN. This role focuses on routine quality audits, product conformance, process review, documentation, and follow‑up reporting within a structured manufacturing environment.

Strong fit for candidates with hands‑on quality inspection, audit, QA/QC, manufacturing quality, or process conformance experience.

Memphis, TN 38118. Onsite role.

$28 to $33/hr.

ASAP, pending background check and drug test.

Expected through December 26, 2026.

• Perform routine quality control audits across manufacturing processes.
• Audit manufacturing methods, sequences, setups, and process steps for conformance.
• Review product quality against required specifications and process standards.
• Conduct audits related to manufacturing processes and maintenance activity.
• Document audit results and report findings to supervisors and management.
• Follow up on audit recommendations and required corrective actions.
• Use basic PC, reporting, math, and problem‑solving skills to support quality documentation.
• Read and follow written instructions, visual aids, work instructions, and quality procedures.

• Experience in quality control, quality inspection, quality audit, QA/QC, manufacturing inspection, or similar hands‑on quality work.
• Ability to inspect or audit products, processes, components, setups, or production activity against defined standards.
• Comfortable documenting findings, reporting issues, and communicating results to supervisors or management.
• Ability to follow SOPs, visual aids, work instructions, checklists, specifications, or quality procedures.
• Basic computer skills, including Windows‑based systems and digital documentation.
• Basic math ability, including decimals, fractions, percentages, ratios, and simple quality calculations.
• Ability to work onsite in Memphis, TN.

• Experience in a manufacturing, production, or process‑driven quality environment.
• Background with medical device, electronics, automotive, aerospace, or other regulated manufacturing.
• Familiarity with ISO, QMS, MES, ERP, inspection systems, audit logs, or production tracking systems.
• Experience with nonconformance documentation, defect reporting, corrective action support, or quality follow‑up.
• Prior title such as Quality Auditor, Quality Inspector, QA Technician, QC Inspector, Quality Technician, Process Auditor, or Manufacturing Quality Specialist.

This role is ideal for someone who enjoys hands‑on quality work in a manufacturing environment and is comfortable checking products and processes against defined standards. The right candidate does not need an exact Quality Auditor title, but should have practical experience with inspection, audit, conformance review, documentation, and quality issue escalation.