GLP Auditor

North Chicago, IL

Post Date: 05/30/2017 Job ID: 22065 Category: Professional

  • Auditing, document review, and project services within a Quality Assurance environment.
  • May assist team during report audits and internal audits according to FDA Good Clinical Practices Regulations, ICH Guidelines and PPGs.
  • May assist team with QC services of Audit Files, spreadsheets, audit reports, as well as assigned projects.
  • Review raw data, protocols and research reports to assure the quality and integrity of the results as well as compliance to protocols, policies, procedures, and applicable GLP regulations/guidance and be able to communicate compliance deficiencies to all appropriate personnel.

  • Good writing and communication skills.
  • Auditing experience in the pharmaceutical industry required.
  • 3-5 year of Experience.

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