Quality Control Inspector II

Medline•Richmond Hill, GA

1d•Onsite

About The Position

Under minimal supervision, the QC Inspector II oversees quality projects, ensures compliance with Medline SOPs, and maintains product integrity at the distribution center. Responsibilities include investigating and documenting held finished goods, managing holds and releases, completing rework assignments, inspecting raw materials and finished goods using various methods, recording inspection results, providing product disposition, ensuring inventory control, performing final inspections, and ensuring compliance with quality procedures and company policies.

Requirements

Ability to apply and remove holds in the system and Q-Tag.
Ability to assess and repackage inbound damaged goods.
Ability to communicate with divisional partners to determine product disposition.
Ability to maintain communication with branch personnel and divisional partners.
Ability to operate material handling equipment (e.g., reach truck, order picker) to manage inventory.
Ability to assist with item adjustments and other inventory-related tasks.
Ability to prioritize and perform recall activities, including stock checks, deviations, relabels, product rework, and pedigree verification.
Ability to coordinate project/rework areas and resources.
Ability to maintain daily reports of held stock using SAP, Excel, and other systems.
Ability to ensure compliance with SOPs and regulations; communicate with management to address non-conformances.
Ability to maintain hazardous waste logs and perform weekly audits.
Ability to use computer systems for communication, reporting, and tracking project time.
Ability to recommend methods to increase efficiency.
Ability to ensure shipments are from licensed vendors and maintain electronic logs.
Ability to perform in-process and final inspections; complete inspection documentation.
Ability to operate test equipment and perform measurements.
Ability to identify defects and initiate non-conforming material reports.
Ability to communicate effectively with quality assurance and production groups.
Ability to verify and approve line start-up and equipment requirements.
Ability to participate in continual improvement and customer satisfaction efforts.
Ability to read and interpret engineering instructions and other documents.
Ability to comply with quality systems, GMP, GDP, OSHA, and company regulations.
Ability to review manufacturing/production documents to ensure accuracy.
Ability to perform line clearance procedures for product release.
Ability to review and approve Engineering Change Notices (ECNs) and substitutions.

Nice To Haves

Individuals who have a passion for making a quality healthcare product in a collaborative and respectful environment.
Those who are enthusiastic about trying new things and learning every day.
A relentless focus on serving the customer every day and are results driven.

Responsibilities

Apply and remove holds in the system and Q-Tag.
Assess and repackage inbound damaged goods.
Communicate with divisional partners to determine product disposition.
Maintain communication with branch personnel and divisional partners.
Operate material handling equipment (e.g., reach truck, order picker) to manage inventory.
Assist with item adjustments and other inventory-related tasks.
Prioritize and perform recall activities, including stock checks, deviations, relabels, product rework, and pedigree verification.
Coordinate project/rework areas and resources.
Maintain daily reports of held stock using SAP, Excel, and other systems.
Ensure compliance with SOPs and regulations; communicate with management to address non-conformances.
Maintain hazardous waste logs and perform weekly audits.
Use computer systems for communication, reporting, and tracking project time.
Recommend methods to increase efficiency.
Ensure shipments are from licensed vendors and maintain electronic logs.
Perform in-process and final inspections; complete inspection documentation.
Operate test equipment and perform measurements.
Identify defects and initiate non-conforming material reports.
Communicate effectively with quality assurance and production groups.
Verify and approve line start-up and equipment requirements.
Participate in continual improvement and customer satisfaction efforts.
Read and interpret engineering instructions and other documents.
Comply with quality systems, GMP, GDP, OSHA, and company regulations.
Review manufacturing/production documents to ensure accuracy.
Perform line clearance procedures for product release.
Review and approve Engineering Change Notices (ECNs) and substitutions.