Precision Quality Inspector – 2nd Shift (Electronics)

Socket.dev; Manteno (IL); On-site; USD 28,000 - 37,000; Full time

Job summary

Gotion Inc. in Manteno, IL seeks a detail-oriented Quality Inspector for the 2nd shift (Mon-Fri 3:00 PM–11:30 PM). You will inspect products using calipers, micrometers, and vision systems to ensure CGMP and HACCP compliance, document results, and support audits.

Requirements include a High School Diploma or GED, manufacturing QC experience, proficiency with Microsoft products, and knowledge of ISO 9001/13485, FDA CGMP. This is a hands-on role contributing to quality improvements.

Qualifications

• High School Diploma or GED equivalent.
• Experience in manufacturing quality control or inspection in electrical, medical devices, or food industries.
• Computer literacy with Microsoft products.
• Knowledge of ISO 9001, ISO 13485, HACCP, FDA CGMP requirements.
• Hands-on with calipers, micrometers, vision systems and CMM.

Responsibilities

• Perform thorough product inspections using precision instruments to verify specifications.
• Document inspection results with data collection and analysis for QA.
• Identify non-conformances and support corrective actions per CGMP/HACCP.
• Participate in root cause analysis to improve quality and efficiency.
• Support internal/external audits with detailed inspection reports.

Skills

Attention to detail

Communication skills

Data analysis

Microsoft Office

Education

High School Diploma or GED

Tools

Calipers

Micrometers

Vision inspection systems

Coordinate Measuring Machines (CMM)

Calypso quality management software

Job description

Gotion Inc. in Manteno, IL seeks a detail-oriented Quality Inspector for the 2nd shift (Mon-Fri 3:00 PM–11:30 PM). You will inspect products using calipers, micrometers, and vision systems to ensure CGMP and HACCP compliance, document results, and support audits.

Requirements include a High School Diploma or GED, manufacturing QC experience, proficiency with Microsoft products, and knowledge of ISO 9001/13485, FDA CGMP. This is a hands-on role contributing to quality improvements.