Quality Control Inspector III

Medline•Lithia Springs, GA

About The Position

The Quality Control Inspector III works under minimal supervision to inspect raw materials, in-process items, and finished goods, including medical products. Inspections use manual, visual, and measurement equipment in accordance with company procedures. The role documents inspection results, provides product disposition, supports inventory control, performs final inspections and line clearance for product release, leads stock checks and inventory rework, and helps ensure compliance with quality procedures and company policies. The inspector establishes and maintains efficient workflows and priorities for Quality Control projects at Medline facilities and supports the QC Supervisor as needed. The role works with production and quality teams to identify defects, address non-conformances, coordinate rework and recall activities, maintain records, and support quality and reliability standards. It also trains and mentors employees and may serve as a backup to the QC Supervisor while interfacing with quality personnel across multiple sites.

Requirements

High school diploma or equivalent is typically required.
At least 2 years of quality control experience in a regulated industry setting.
Proficiency in reading, writing, speaking, and understanding English.
Strong attention to detail.
Excellent vision, including close and distance vision, depth perception, and ability to adjust focus.
Basic math skills, including addition, subtraction, and conversion of fractions to decimals.
Basic computer skills, including generating Non-Conforming Material Reports (NCMRs) or certificates as needed and using Microsoft Office Suite, including Outlook, Word, and Excel.
Ability to work in hot and cold environments.
Ability to sit, walk, or stand for prolonged periods and frequently twist and bend.
Ability and willingness to wear PPE or company-issued gowns for extended periods.
Ability to lift up to 50 lbs.
Ability to prioritize tasks quickly in a fast-paced manufacturing environment.
Ability to process relevant details, assess their importance, prioritize them, and draw concise conclusions.
Knowledge of quality regulations such as GMP, GDP, ISO, or 21 CFR 820 and 210–211.

Nice To Haves

At least 4 years of quality control experience in a medical device and/or drug manufacturing setting.

Responsibilities

Conduct timely in-process and final product inspections according to company procedures and complete required documentation.
Operate test equipment and use measurement tools, including rulers, tape measures, and scales, in accordance with standard operating procedures.
Identify defects and initiate non-conforming material reports in accordance with company policy or Accepted Quality Limits (AQL).
Communicate inspection results, defects, and non-conforming reports to quality assurance and production teams.
Verify and approve line start-up and equipment requirements according to company procedures.
Participate in continuous improvement and customer satisfaction initiatives.
Read and interpret engineering instructions and production documents, including Bills of Material, pick sheets, substitutions, and Engineering changes.
Comply with OSHA regulations and Medline rules, including Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
Review manufacturing and production documents for accuracy and completeness.
Perform line clearance procedures for final product release.
Review and approve floor-initiated Engineering Change Notices (ECNs) and substitutions.
Lead stock checks and inventory rework to identify and isolate damaged components.
Prioritize and coordinate recall activities, stock checks, deviations, and reworks.
Manage project and rework areas and resources.
Maintain daily reports of held stock using SAP, Excel, and other systems.
Ensure compliance with Medline SOPs and regulations and communicate with management about non-conformances.
Maintain hazardous waste logs and perform weekly audits.
Use computer systems for communication, reporting, product investigation, and project tracking.
Recommend methods, procedures, and standards to improve efficiency.
Ensure shipments come from licensed vendors and maintain electronic license logs.
Serve as backup to the QC Supervisor and interface with quality personnel across multiple sites.
Contribute to corporate functions such as workload distribution and project tracking.
Train and mentor new and existing Quality, Manufacturing, or Operations employees on procedures to support proper workflow and project completion.