Quality Control Inspector III

Medline Industries, LP • Lithia Springs, GA

3d • $25 - $36

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, using 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, and leads stock checks and inventory rework. It also helps establish and maintain efficient workflows and priorities for Quality Control projects at Medline facilities, supporting the QC Supervisor and promoting adherence to quality and reliability standards.

The position coordinates with quality assurance, production, management, and personnel across multiple sites. It supports recalls, deviations, rework, continuous improvement, customer satisfaction, employee training, and corporate workload and project tracking. The role also maintains inspection, inventory, and hazardous-waste records and ensures compliance with applicable procedures and regulations.

Requirements

• High School Diploma or equivalent, 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 vision, distance vision, depth perception, and ability to adjust focus.
• Basic math skills, including addition, subtraction, and converting fractions to decimals.
• Basic computer skills, including generating Non-Conforming Material Reports (NCMRs) or certificates as necessary, and proficiency with 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 personal protective equipment (PPE) or company-issued gowns for extended periods.
• Ability to lift up to 50 lbs.
• Ability to quickly prioritize tasks in a fast-paced manufacturing environment.
• Ability to process relevant details, understand and prioritize their importance, 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 and complete required documentation.
• Operate test equipment and perform measurements using tools such as rulers, tape measures, and scales according to standard operating procedures.
• Identify defects and initiate non-conforming material reports according to 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 Engineering Change Notices (ECNs) and floor-initiated 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 held-stock reports using SAP, Excel, and other systems.
• Ensure compliance with Medline SOPs and regulations and communicate with management to address 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 are 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.

Benefits

• Competitive total rewards package.
• Continuing education and training.
• Health insurance for eligible employees.
• Life insurance for eligible employees.
• Disability benefits for eligible employees.
• 401(k) contributions.
• Paid time off.
• Access to the Employee Assistance Program, Employee Resource Groups, and the Employee Service Corp for employees working fewer than 30 hours per week.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED