Quality Control Inspector – FDA/ISO Compliance

Mac-Medical-3; 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-3 seeks a detail-oriented Quality Control Inspector to ensure products meet high quality standards and regulatory requirements. You will inspect in-process and finished goods, examine supplier materials, and perform tests with various instruments.

Responsibilities include documenting results, conducting internal audits (FDA CFR 21, ISO 9001:2008), and collaborating with teams to improve quality. This role requires reading product prints and strong data skills.

Qualifications

• 1–2 years of QA experience with FDA CFR 21 and ISO 9001:2008.
• Excellent communication and teamwork abilities.
• Strong data analysis and documentation skills.
• Ability to read product prints and specifications.
• Experience with audits and regulatory standards.

Responsibilities

• Ensure quality of manufactured goods and in-process inspections.
• Examine materials from suppliers before sending to production.
• Inspect components, subassemblies, and assemblies.
• Perform tests using instruments and equipment as required.
• Record pass/fail data in inspection databases.
• Conduct internal audits for FDA CFR 21 and ISO 9001:2008.
• Read and interpret product prints/specifications.
• Utilize test equipment such as thermometers and voltmeters.
• Collaborate with teams to maintain quality standards.

Skills

Quality Assurance

Regulatory knowledge

Interpersonal skills

Customer focus

Planning & organization

ERP systems

Tools

Excel (Pivot Tables)

Microsoft Office

SharePoint

Access database

Intuitive ERP

Job description

Mac-Medical-3 seeks a detail-oriented Quality Control Inspector to ensure products meet high quality standards and regulatory requirements. You will inspect in-process and finished goods, examine supplier materials, and perform tests with various instruments.

Responsibilities include documenting results, conducting internal audits (FDA CFR 21, ISO 9001:2008), and collaborating with teams to improve quality. This role requires reading product prints and strong data skills.