Covance

  • GLP QA Officer

    Job Location(s) US-IN-Greenfield
    Job Number
    2018-19428
    Job Category
    Quality Assurance
    Position Type
    Full-Time
  • Job Overview

    Do you appreciate the importance of paying attention to details? Are you an organized person who can work independently and drive data integrity? Are you familiar with GLP/GCP regulations?

     

     

    If you are looking to grow your career as an auditor, consider joining Covance as a Quality Assurance Officer. In this position you will perform protocol, data, and report review and in-lab inspections to verify compliance with applicable SOPs and regulatory requirements (GLP/GCP) as you:

     

    • Participate in internal facility and supplemental inspections
    • Deliver training in basic quality and regulatory matters and perform SOP reviews
    • Perform study sign-off activities including QA statement preparation and report finalization
    • Identify opportunities for process improvement and harmonization efforts that promote best practices 

     

    This position is office-based in Greenfield, IN.

    Education/Qualifications

    • A Bachelor’s degree, preferably in science or a related field is highly preferred

    Experience

    • At least 2 years of experience working in a GLP/GCP regulated environment with some auditing experience preferred
    • Strong drive for process optimization and data integrity
    • Excellent communication and interpersonal skills with great attention to detail
    • Experience working in the CRO/Pharma industry highly preferred

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