Quality Inspector – 2nd Shift, Precision QC

Gotion, Inc.; Manteno (IL); On-site; USD 27,000 - 39,000; Full time

Benefits offered by this job

Calypso familiarity

Job summary

Gotion Inc. seeks a detail-oriented Quality Inspector to ensure products meet strict quality standards in a fast-paced manufacturing environment.

The role emphasizes accurate use of calipers, micrometers, vision systems, and CMMs, with strong documentation and data analysis to support QA initiatives. Responsibilities include identifying non-conformances, assisting with corrective actions, and participating in audits, while aligning with ISO 9001/13485, HACCP, and FDA CGMP expectations.

Qualifications

• High School Diploma or GED is required.
• Experience in manufacturing quality control or inspection roles in electrical, medical devices, or food industries.
• Computer literacy with Microsoft products.
• Knowledge of ISO 9001, ISO 13485, HACCP, FDA CGMP standards.
• Hands-on experience with calipers, micrometers, vision systems, or CMMs.
• Ability to analyze data, identify trends and drive process improvements.
• Excellent attention to detail and clear documentation skills.

Responsibilities

• Perform inspections using precision instruments to verify specifications.
• Meticulously document inspection results and data.
• Identify non-conformances and support corrective actions per CGMP/HACCP.
• Assist in root-cause analysis to improve quality and efficiency.
• Support internal and external quality audits with thorough reports.

Skills

Quality inspection

Data analysis

Documentation

Measurement tools

Attention to detail

Education

High School Diploma or GED

Tools

Calipers

Micrometers

Vision inspection systems

CMM

Job description

Gotion Inc. seeks a detail-oriented Quality Inspector to ensure products meet strict quality standards in a fast-paced manufacturing environment.

The role emphasizes accurate use of calipers, micrometers, vision systems, and CMMs, with strong documentation and data analysis to support QA initiatives. Responsibilities include identifying non-conformances, assisting with corrective actions, and participating in audits, while aligning with ISO 9001/13485, HACCP, and FDA CGMP expectations.