GLP QA Officer

Covance Inc Located in: Greenfield,  Indiana
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Covance Inc Biotechnology Jobs Pharmaceutical Careers
 

JOB DESCRIPTION

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.

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

COMPANY INFORMATION

Covance Inc. is proud to be the only drug development company with a full range of research and development services—from lead optimization, to commercialization and life cycle management. Covance, headquartered in Princeton, NJ, is the drug development business of LabCorp with global operations in more than 30 countries.

JOB INFORMATION

Seniority Level:
Experienced - Not Management
Function:
  Quality
Preferred Industry Background:
 
Managing a team of:
N/A
Required Travel:

Base Salary:
Confidential
Bonus:
Benefits:
Other Compensation: