Cleanroom QC Inspector I – Medical Devices

Medline Industries, Inc.; Eagan (MN); On-site; USD 26,000 - 37,000; Full time

Benefits offered by this job

Health insurance

Life and disability insurance

401(k) contributions

Paid time off

Job summary

Medline Industries, LP is seeking a QC Inspector to support on the clean room production floor. You will inspect, review quality records, and assist with investigations to drive timely quality issue resolutions.

The role contributes to product quality, regulatory compliance, and continuous improvement initiatives, with a focus on risk reduction and CAPA effectiveness within GMP/ISO contexts.

Qualifications

• High school diploma or equivalent required.
• Ability to read, write, speak and understand English.
• Detail-oriented with basic math/measurement skills.
• Able to lift up to 50 lbs and work in PPE.

Responsibilities

• Perform incoming, in-process, and finished product inspections using approved sampling plans and methods.
• Review DHRs, batch records, sterilization docs, 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/verification activities including process and test method validation.
• Support supplier quality activities including receiving inspections and issue tracking.
• Maintain quality metrics and prepare reports for management review.
• Assist during internal, customer, regulatory, and certification audits.
• Comply with SOPs, Quality Systems, OSHA guidelines, and Medline rules.

Skills

English proficiency

Attention to detail

Math skills

PPE safety

Lifting 50 lbs

Education

High School Diploma or equivalent

Job description

Medline Industries, LP is seeking a QC Inspector to support on the clean room production floor. You will inspect, review quality records, and assist with investigations to drive timely quality issue resolutions.

The role contributes to product quality, regulatory compliance, and continuous improvement initiatives, with a focus on risk reduction and CAPA effectiveness within GMP/ISO contexts.