Covance GLP QA Officer II in Indianapolis, Indiana

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 initiate and update local SOPs

  • Perform study sign-off activities including QA statement preparation and report finalization

  • Identify opportunities for process improvement and harmonization efforts that promote best practices

  • Evaluate responses to inspection reports, follow-up as appropriate, and ensure resolution

This position is office-based in Indianapolis.

Education/Qualifications

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

Experience

  • At least 2 years of experience as a quality auditor in a GxP regulated environment

  • 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

Job Number 2018-20268

Job Category Quality Assurance

Position Type Full-Time

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.