Quality Control Reviewer- Pharma

Covance Inc Located in: Chantilly,  Virginia
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Covance Inc Biotechnology Jobs Pharmaceutical Careers


Quality Control Reviewer/Study Coordinator

Advance your career with a global leader


Do you appreciate the importance of paying attention to details? Do you have an interest in and a strong understanding of science? Are you good with mathematical calculations?


If you are looking to grow your career while applying your math and science skills to support laboratory data review, you should consider joining Covance as a Quality Control (QC) Reviewer in our office in Chantilly, VA. In this position, we’re looking for someone to accomplish several responsibilities, such as:


  • Review laboratory data to ensure quality standards are met and to verify compliance with applicable SOP and regulatory requirements (GLP)
  • Track reviewed documents and noted errors following up to ensure document correction and completion  
  • Monitor citation trends and perform follow-up actions with respondents or management to prevent recurring citations, problems, and  errors
  • Maintain and seek to expand a strong working knowledge of SOP and regulatory requirements and other guidance documents
  • Assist co-workers and internal customers with interpretation and understanding of SOP and regulatory requirements and other guidance documents, as applicable
  • Identity areas for process improvement


This position is office based in our Chantilly, VA facility.



Why QC Reviewers choose to work at Covance


  • Join a global company for career development and growth opportunities
  • Identify unique solutions to make a direct impact in healthcare
  • Partner with and learn from compassionate colleagues and industry leaders


What we’re looking for



QC Reviewers are most successful at Covance with:


  • A Bachelor’s degree in science or a related field
  • Knowledge of current regulatory standards
  • Knowledge and an interest in scientific data
  • Pharmaceutical or CRO experience highly preferred
  • Proficiency in Microsoft Office applications


Why Covance


Bringing new medicines to market requires bold ideas. That’s why we empower our exceptional people with mentoring, in-depth training and tailored career planning. You’ll have the opportunity to own your career journey and develop alongside supportive, industry leaders who are passionate about your individual success. At Covance, you’ll discover your own extraordinary potential as you explore diverse projects and unique career paths across the drug development spectrum.


Join us and discover your energized purpose as we transform possibilities into reality for our clients—and your career.



Ready to join us? Let’s get started.


•Bachelor of Science (BS) degree in science.

•Experience may be substituted for education.

•Efficient use of word processing software, database, spreadsheet, and specialized software.

•Proficient in concise writing; writing should require little or no external review or edit.

•Adherence to grammar, punctuation, composition, and spelling according to company standard conventions.

•Experience on a variety of studies performed in the department and exposure to a diverse client base.

•Knowledge of regulatory agency guidelines.

•Two years of Quality Review or Study Coordinator experience.

•Excellent communication, presentation, and interpersonal skills.

•Excellent attention to detail. Efficient in prioritizing and managing time.

Not ready to apply? Connect with us to join our talent community.



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.


Seniority Level:
Experienced - Not Management
  Clinical Research / Affairs,  R&D / Science,  Medical Affairs
Preferred Industry Background:
Managing a team of:
Required Travel:

Base Salary:
Other Compensation: