Covance GLP QA Officer in Greenfield, Indiana
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
Job Number 2018-19428
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.