Senior GCP QA Auditor
Advance your career with a global leader
Do you appreciate the importance of paying attention to details? Can you maintain flexibility in a changing environment?
If you are looking to grow your career, you should consider joining Covance as a Senior Quality Assurance (QA) Auditor. In this position, you will support Senior Management in maintaining robust quality systems while assuring regulatory compliance within Clinical Pharmacology (CPS) as you:
An office based candidate is highly preferred out of our offices in Dallas, TX; Madison, WI; or Daytona Beach, FL. Internal candidates may be considered in other US locations.
Working and growing at Covance
At Covance, you’ll work in our energizing environment and support our client-centric solutions as one the world's largest and most comprehensive drug development services companies.
You will receive 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 Senior QA Auditors choose to work at Covance
Get to know Covance
Beyond excellent compensation and benefits as a Senior QA Auditor, 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
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.
A minimum of 5 years of experience working in the Pharma or CRO industries with at least 1 year of experience in clinical QA is required (GCP preferred). Experience in early phase clinical trials (Phase I – IIa) is highly desired and preferable.
Other essential requirements for this position include: