Entry-Level Quality Control Inspector – Clean Room

Medline Industries, LP; Eagan (MN); On-site; USD 25,000 - 37,000; Full time

Benefits offered by this job

Health insurance

401(k) contributions

Paid time off

Job summary

Medline Industries, LP is seeking a QC Inspector to uphold quality on the clean room production floor, performing inspections, reviewing records, and assisting investigations to rapidly resolve quality issues.

You will support product release activities and CAPA processes, ensuring complete and accurate quality documentation while helping drive GMP/ISO compliance and continuous improvement initiatives.

Qualifications

• High School Diploma or equivalent required.
• No experience required.
• Willingness to work in PPE and manufacturing environments.

Responsibilities

• Perform incoming, in-process, and finished product inspections using approved sampling plans and methods.
• Review DHRs, batch records, sterilization documentation, and manufacturing records for completeness and compliance.
• Support release activities for finished products and ensure quality documentation is complete and accurate.
• Assist with investigations related to nonconformances, deviations, complaints, supplier issues, and corrective actions.
• Support CAPA implementation, effectiveness verification, and follow-up activities.
• Assist with validation and verification activities including process and test method validation and sterilization studies.
• Maintain quality metrics and prepare reports for management review and quality performance monitoring.
• Assist during internal, customer, regulatory, and certification audits.
• Comply with SOPs, Quality Systems, OSHA guidelines, and Medline rules.

Skills

Attention to detail

English proficiency

Basic math

Prioritization

Education

High School Diploma or equivalent

Tools

Basic computer skills

Job description

Medline Industries, LP is seeking a QC Inspector to uphold quality on the clean room production floor, performing inspections, reviewing records, and assisting investigations to rapidly resolve quality issues.

You will support product release activities and CAPA processes, ensuring complete and accurate quality documentation while helping drive GMP/ISO compliance and continuous improvement initiatives.