Quality Spec & Documentation Specialist

Medline Industries, Inc. in; Chicago (IL); On-site; USD 67,000 - 101,000; Full time

Job summary

Medline Industries, LP is seeking a Spec Quality Project Management role focusing on quality system subsections such as device master records and customer complaints. You will build and maintain quality documentation and ensure procedures meet specifications.

The role requires at least 2 years in quality, a bachelor’s in a related field, and ability to collaborate across internal and external teams while following FDA/ISO standards and traveling up to 10% as needed.

Qualifications

• Bachelor's degree in Engineering, Science, Math or related field.
• Minimum 2 years ofQuality experience.
• Experience developing quality documentation and processes.

Responsibilities

• Assist in developing and implementing processes, reports and procedures within specialization.
• Collaborate with internal/external groups to ensure FDA/ISO compliance.
• Facilitate meetings with global units to manage project requirements and deadlines.
• Review documentation for completeness and accuracy to meet specifications.
• Make recommendations based on analysis to improve quality and customer experience.

Skills

Time management

MS Office

Excel

Documentation

Quality assurance

FDA ISO knowledge

Collaboration

Travel readiness

Education

Bachelor's degree in Engineering/Science/Math

Job description

Medline Industries, LP is seeking a Spec Quality Project Management role focusing on quality system subsections such as device master records and customer complaints. You will build and maintain quality documentation and ensure procedures meet specifications.

The role requires at least 2 years in quality, a bachelor’s in a related field, and ability to collaborate across internal and external teams while following FDA/ISO standards and traveling up to 10% as needed.