Quality Control Inspector II - West Jefferson, OH (Biotech)

Job Summary

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.

Job Description

MAJOR 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.

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:

$19.75 - $27.75 Hourly

The actual salary will vary based on applicant's location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold.

Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp.

Every day, we're focused on building a more diverse and inclusive company, one that recognizes, values and respects the differences we all bring to the workplace. From doing what's right to delivering business results, together, we're better. Explore our Diversity, Equity and Inclusion page here.

Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.