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in Kansas City, MO

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Hours Full-time, Part-time
Location Kansas City, Missouri

About this job

Job Description

Job Description
Primary Responsibilities Quality Auditors:
  • Conducts manufacturing process audit.
  • Provides timely, detailed reports and photographic evidence
Certifications/Experience Requirements:
  • ISO 9001:2015 Auditor
  • ISO 13485:2016 Auditor
  • 21 CFR 820 (GMP)
  • Has to conduct audit in Plastics/ Manufacturing / QMS / Supplier Quality Audits
Experience Requirements:
  • Preferred experience in conducting Audits in Medical Device manufacturing, Goods Manufacturing
  • Proficient in Microsoft Office suite of tools, Specifically Word, Excel, Power Point.
  • Must possess appropriate mathematical and analytical skills to determine acceptability of product(s) based on established criteria
  • Self-motivated with the ability to self-manage (set and achieve goals) and work with limited supervision.
  • Organizational skills with attention to detail
Job type: 1099 contract

Working setting: This is an in-person, daytime 8 hours shift job, workweek assignment.

Ability to commute to North Kansas City, MO