Manufacturing Quality Auditor (ISO/GMP)

GXO Logistics, Inc.; Tracy (CA); On-site; USD 25,000 - 36,000; Full time

Benefits offered by this job

Health insurance

401(k)

Life insurance

Disability insurance

Job summary

GXO Logistics, Inc. is seeking a Quality Specialist for a weekend afternoon shift in Tracy, CA. You will audit manufacturing processes, verify ISO policy adherence, and support quality and operations teams to ensure product conformance.

Responsibilities include documenting findings, training staff on procedures, and participating in special QA projects. The role requires strong attention to detail and GMP awareness in a fast-paced warehouse environment.

Qualifications

• Experience interpreting graphs and data.
• Proficiency with Microsoft Office applications.
• Ability to perform basic arithmetic in all units of measure.
• Ability to read and understand simple instructions and memos.
• At least 1 year in documentation writing.
• At least 1 year in site and employee assessments.

Responsibilities

• Work with quality assurance, manufacturing operations, and inventory control.
• Perform random in-process audits as directed by QA leadership.
• Inspect finished products, in-process items, and incoming materials for conformance.
• Investigate issues and communicate findings to supervisors.
• Document audit findings in the quality database system.
• Train teams on procedures and update work instructions as needed.
• Support special projects and provide management reports on findings.
• Adhere to the company quality policy and good manufacturing practices.

Skills

Graphs interpretation

Microsoft Office

Math in all units

Reading comprehension

Documentation writing

Site and employee assessments

Education

High school diploma or equivalent

Job description

GXO Logistics, Inc. is seeking a Quality Specialist for a weekend afternoon shift in Tracy, CA. You will audit manufacturing processes, verify ISO policy adherence, and support quality and operations teams to ensure product conformance.

Responsibilities include documenting findings, training staff on procedures, and participating in special QA projects. The role requires strong attention to detail and GMP awareness in a fast-paced warehouse environment.