Covance

Quality Assurance Officer , GLP/GCP

US-WI-Madison
Job Number
2017-13395
Job Category
Administration/Clerical
Position Type
Full-Time

Job Overview

Quality Assurance Officer

Grow your career with a global leader

 

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 Madison, WI.

 

Working and thriving at Covance

 

As part of the global QA team, you’ll work in our fast-paced environment and contribute to our client-centric solutions in one the world's largest and most comprehensive drug development services companies.

 

We offer a competitive compensation package with medical and dental insurance, tuition reimbursement, a 401(k) plan with a generous company match, along with short and long-term disability and life insurance.

 

Why QA Officers choose to work at Covance

 

  • Join a global company with many opportunities for career growth
  • Make a direct impact in healthcare and the lives of patients
  • Partner with and learn from inspiring colleagues and industry leaders

 

What we’re looking for

 

QA Officers are the most successful at Covance with:

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

 

Get to know Covance

 

Beyond excellent compensation and benefits as a Quality Assurance Officer, joining Covance opens the door to many career opportunities. Learn about what’s possible for your career when a company truly invests in you at http://careers.covance.com/possibilities.html

 

Why Covance

 

At Covance, it’s our people that make us great – it’s what our clients, our partners and, most importantly, what our employees say. Here, you’ll have the opportunity to lead exceptional people with diverse viewpoints. You’ll discover your own extraordinary potential as you drive strategy and build an even stronger organization with industry leaders from early development to the clinic and beyond. Through your everyday work and an energized purpose, you’ll advance science and impact the lives of countless individuals.

 

Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients, our team—and you.

 

Ready to join us? Let’s get started.

 

Education/Qualifications

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

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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