Quality Control Inspector Iii

Medline; Lithia Springs (GA); Sur place; USD 34 000 - 49 000; Plein temps

Résumé du poste

Medline is seeking a QC Inspector III to inspect raw materials, in-process items, and finished goods with manual and measurement tools. You will document results, disposition products, and ensure inventory control under GMP/GDP guidelines.

You will lead inspections, support line starts, and participate in continuous improvement initiatives in a fast-paced medical device manufacturing environment.

Qualifications

• At least 2 years of quality control experience in a regulated industry setting.
• At least 4 years of quality control experience in medical device and/or drug manufacturing setting (preferred).

Responsabilités

• Conduct timely in-process and final inspections of products following company procedures and complete necessary documentation.
• Operate test equipment and perform measurements with rulers, tape measures, scales per SOPs.
• Identify defects and initiate non-conforming material reports according to policy and AQL.
• Communicate inspection results, defects, and non-conforming reports with QA and production teams.
• Verify and approve line start-up and equipment requirements per procedures.
• Lead stock checks and inventory rework to identify damaged components.

Connaissances

English proficiency

Attention to detail

Vision

Math skills

MS Office skills

Formation

High School Diploma

Outils

SAP

Microsoft Excel

Description du poste

Job Summary

The QC Inspector III, working under minimal supervision, inspects raw materials, in-process items, and finished goods (including medical products) using manual, visual, and measurement equipment per company procedures. Key duties include documenting quality inspection results, providing product disposition, ensuring inventory control, performing final inspections (including line clearance and product release), leading stock checks and inventory rework, and ensuring compliance with quality procedures and company policies. Additionally, the QC Inspector III establishes and maintains efficient workflow and prioritization for Quality Control projects at Medline facilities, supporting the QC Supervisor as needed to ensure adherence to quality and reliability standards.

Job Description

MAJOR RESPONSIBILITIES:

• Conduct timely in-process and final inspections of products, following company procedures and completing necessary documentation.
• Operate test equipment and perform measurements using tools like rulers, tape measures, and scales, adhering to standard operating procedures.
• Identify defects and initiate non-conforming material reports during inspections, following company policy or Accepted Quality Limits (AQL).
• Communicate inspection results, defects, and non-conforming reports effectively with quality assurance and production teams.
• Verify and approve line start-up and equipment requirements as per 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's rules, including Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Review manufacturing and production documents to ensure accuracy and completeness.
• Perform line clearance procedures for final product release.
• Review and approve Engineering Change Notices (ECNs) and substitutions initiated on the floor.
• Lead stock checks and inventory rework to identify and isolate damaged components.
• Prioritize and coordinate recall activities, stock checks, deviations, and reworks.
• Manage project/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 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 logs of licenses.
• Serve as backup to the QC Supervisor and interface with quality personnel across multiple sites.
• Contribute to corporate functions like workload distribution and project tracking.
• Train and mentor new and existing Quality, Manufacturing, or Operations employees on procedures to ensure proper workflow and project completion.

MINIMUM JOB REQUIREMENTS:

Education:

• Typically requires High School Diploma or equivalent.

Certification / Licensure:

• None

Work Experience:

• At least 2 years of quality control experience in a regulated industry setting.

Knowledge / Skills / Abilities:

• Proficiency in reading, writing, speaking, and understanding English.
• Strong attention to detail.
• Excellent vision abilities, including close vision, distance vision, depth perception, and the ability to adjust focus.
• Basic math skills, including addition, subtraction, and converting fractions to decimals.
• Basic computer skills, including the ability to generate Non-Conforming Material Reports (NCMRs) or certificates as necessary, and proficiency with Microsoft Office Suite (Outlook, Word, Excel, etc.).
• Ability to work in both hot and cold environments.
• Capability to sit, walk, or stand for prolonged periods, with frequent twisting and bending.
• Willingness to work in 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.
• Competence in processing all relevant details, understanding and prioritizing their importance, and drawing concise conclusions.
• Knowledge of quality regulations such as GMP, GDP, ISO, or 21CFR 820, 210 - 211.

PREFERRED JOB REQUIREMENTS:

Education:

• None

Certification / Licensure:

• None

Work Experience:

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

Knowledge / Skills / Abilities:

• None

Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.

The anticipated salary range for this position:

$24.50 - $35.50 Hourly

The actual salary will vary based on applicant's location, education, experience, skills, and a