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