Covance

Quality Assurance Compliance Advisor - GLP / GCP Labs

Job Location(s) US-IN-Indianapolis
Job Number
2017-13162
Job Category
Quality Assurance
Position Type
Full-Time

Job Overview

Quality Assurance Compliance Advisor

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 while applying your auditing skills to support our regulatory requirements, you should consider joining Covance as a Quality Assurance (QA) Compliance Advisor in our Indianapolis, IN office. In this position, we’re looking for someone to accomplish several responsibilities, such as:

 

 

  • Hold and host audits with our clients
  • Perform internal audits and liaise with our operational groups
  • Interpret regulatory requirements and quality standards
  • Craft local procedures and deliver training materials to QA teams
  • Train auditors on regulatory requirements

 

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 QA Compliance Advisors 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

 

 

A minimum of 4 years of quality auditing experience with GLP/GCP in a lab-based environment is required. ISO 15189 experience in medical laboratories preferred. Other essential requirements for this position include:

 

  • BA/BS four-year degree (science-related field desirable)
  • Pharmaceutical or CRO experience
  • Experience with CAP requirements
  • Experience hosting audits
  • Strong communication skills
  • Proficiency in Microsoft Office applications
  • Experience using TrackWise QMS software (desirable)

 

 

Get to know Covance

 

Beyond excellent compensation and benefits as a QA Compliance Advisor, 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

 

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.

Education/Qualifications

  • BA/BS four-year degree (science-related field desirable)
  • Pharmaceutical or CRO experience
  • Experience with CAP requirements
  • Experience hosting audits
  • Strong communication skills
  • Proficiency in Microsoft Office applications
  • Experience using TrackWise QMS software (desirable)

Experience

A minimum of 4 years of quality auditing experience with GLP/GCP in a laboratory environment is required. ISO 15189 experience in medical laboratories preferred. 

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