Spec Quality

Medline Industries LP

Not specified
Bachelor's degree in engineering or science
2 years of quality experience
Fda and iso compliance knowledge
Medline Industries LP is seeking a Spec Quality professional to enhance their Quality Management System by maintaining quality documentation and processes. The role requires experience in Quality, collaboration with various teams, and knowledge of FDA and ISO standards

Job Summary

  • This role specializes in specific subsections of the Quality Management System such as Device Master Records and customer complaints.
  • The incumbent must collaborate with internal and external groups to ensure compliance with FDA, ISO, and internal requirements.
  • Responsibilities include reviewing documentation for completeness and accuracy while making recommendations to improve quality standards.

Matching Summary

Match Score: 75

Medline Industries LP is seeking a Spec Quality professional to enhance their Quality Management System by maintaining quality documentation and processes. The role requires experience in Quality, collaboration with various teams, and knowledge of FDA and ISO standards.

Skills & Requirements

Must-have

  • Bachelor's degree in Engineering or Science
  • 2 years of Quality experience
  • FDA and ISO compliance knowledge
  • MS Office Suite proficiency
  • Intermediate Excel skills

Nice-to-have

  • Global business unit collaboration
  • Project deadline management
  • Complex problem solving abilities
  • ERP system analysis experience

Key Requirements

  • Bachelor's degree required
  • Minimum 2 years Quality experience
  • Working knowledge of 21 CFR 820 and ISO 13485

Work Rights

Not specified

Tailored Resume

Cover Letter