Quality Inspector in Durham, NC at Volt

Date Posted: 8/10/2018

Job Snapshot

  • Employee Type:
    Contingent
  • Location:
    Durham, NC
  • Duration:
    72 weeks
  • Date Posted:
    8/10/2018
  • Job ID:
    131359
  • Pay Rate
    $17.0 - $18.0/Hour
  • Contact Name
    Volt Branch
  • Phone
    919/829-1660

Job Description

Volt Workforce Solutions offers full-service staffing and talent management consulting to help local, regional, national, and international companies. Through niche recruiting expertise and project management, VWS delivers solutions in IT, Technology, Engineering, Accounting, Administrative, Call Center, Human Resources, Technical and Creative Communication, and Manufacturing.

Volt is an equal opportunity employer.

We are actively seeking an AQL Inspector for our client in Durham, NC. This is a great opportunity to work with a dynamic company that is a global leader in the field of in vitro diagnostics.

The duration of this assignment is up to six months.

The AQL Inspector is responsible for performing the inspection of finished products in accordance with specified sampling plans and ensuring that specifications are met.

  • Perform QA Product Inspection on the Packaging line products;
  • Perform Real Time Review of Packaging documentation as required;
  • Support quality investigation activities, including but not limited to customer complaints, non-conformance investigations, and CAPAs;
  • Track/report status of documentation errors to management on a timely basis;
  • Support Internal/External Audits as required;
  • Support continuous improvement projects.

Requirements:

Must be able to work 7:00am - 7:30pm on a 2-2-3 schedule.

  • Associate’s Degree in production process-related field desired, plus a minimum of three (3) years of progressively responsible and related experience working in a production facility, or 5 years relevant experience in a similar position in lieu of degree;
  • Experience in an FDA regulated, GMP environment with knowledge of Good Documentation Practices is required;
  • Knowledge of FDA/cGMP regulations is preferred;
  • Familiarity with relevant Domestic and International Regulations and Industry Standards (e.g. ISO, FDA QSR).