Quality Control Inspector — Data-Driven & ISO 9001 Expert

MAC Medical, Inc.; Millstadt (IL); On-site; USD 28,000 - 32,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Life insurance

Short-term disability

Long-term disability

Paid time off

Paid holidays

Employee assistance program

401(k)

401(k) matching

Job summary

MAC Medical, Inc. is seeking a detail-oriented Quality Control Inspector in Millstadt, IL to ensure products meet high quality standards and regulatory requirements. You will perform inspections at all stages, run tests with precision, and document results in our QA databases.

The role requires familiarity with FDA CFR 21 and ISO 9001:2008, strong analytical skills, and the ability to read complex product prints. A collaborative team environment and accurate reporting are essential.

Qualifications

• 1–2 years of experience in QA with regulatory awareness.
• Ability to read product prints / specifications.
• Strong data analysis and inspection testing.
• Capable of internal audits (FDA CFR 21, ISO 9001:2008).

Responsibilities

• Ensure quality of manufactured goods.
• Inspect goods in process and finished product.
• Examine materials from suppliers before production.
• Inspect components, subassemblies, and assemblies.
• Perform tests using instruments and equipment.
• Test, measure, and analyze products.
• Record pass/fail data in Quality Inspection Databases.
• Read and understand product prints / specifications.
• Conduct internal audits to ensure compliance with codes.
• Perform other duties as assigned.

Skills

Quality Assurance

FDA CFR 21

ISO 9001:2008

Interpersonal skills

Communication skills

Excel (Pivot Tables)

ERP systems (Intuitive ERP)

Tools

Excel (Pivot Tables)

Microsoft Office

SharePoint

Access database

Intuitive ERP

Job description

MAC Medical, Inc. is seeking a detail-oriented Quality Control Inspector in Millstadt, IL to ensure products meet high quality standards and regulatory requirements. You will perform inspections at all stages, run tests with precision, and document results in our QA databases.

The role requires familiarity with FDA CFR 21 and ISO 9001:2008, strong analytical skills, and the ability to read complex product prints. A collaborative team environment and accurate reporting are essential.