Covance

Computer Systems Quality Specialist , GxP

US-IN-Indianapolis
Job Number
2017-15110
Job Category
Quality Assurance
Position Type
Full-Time

Job Overview

Computer Systems Quality Specialist

Thrive in a collaborative environment and advance your career

 

Are you a leader known for building effective working relationships? Are you an organized person who can work independently and drive data integrity? Can you ensure systems compliance to quality standards across our global GCP/GLP-regulated environment?

 

 

If you are looking to grow your career while applying your leadership skills to support the quality of our computer systems and data integrity, consider joining Covance as a Computer Systems Quality Specialist. In this role, you will audit System Life Cycle (SLC) documents against CGP regulations in a clinical laboratory setting and consult with internal clients to implement and improve processes that drive system compliance and data integrity as you:

  • Drive system compliance and data integrity, set expectations and goals, and implement and optimize processes
  • Perform computerized system and facility inspections
  • Identify process improvement opportunities, develop and revise SOPs, and lead departmental initiatives
  • Support, participate in, and host client, regulatory, and vendor audits
  • Partner with the IT and operational departments to provide system resolutions
  • Provide QA sign off on system release, track system trends, and complete risk assessments

 

This position is office-based in Indianapolis, IN.

 

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 Quality Specialists 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

 

 

The qualifications of an ideal candidate include:

  • A Bachelor’s degree, preferably in science or a related field
  • At least 2 years of experience working in a similar position within a GxP regulated environment
  • Strong drive for process optimization and data integrity
  • Demonstrated leadership skills with a proven track record of driving continuous improvement
  • Excellent communication and interpersonal skills with the ability to influence others with impact
  • Outstanding experience with client satisfaction and problem solving solutions
  • Experience working in the CRO/Pharma industry highly preferred

 

Get to know Covance

 

Beyond excellent compensation and benefits as a Computer Systems Quality Specialist, 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 similar position within a GxP regulated environment
  • Strong drive for process optimization and data integrity
  • Demonstrated leadership skills with a proven track record of driving continuous improvement
  • Excellent communication and interpersonal skills with the ability to influence others with impact
  • Outstanding experience with client satisfaction and problem solving solutions
  • Experience working in the CRO/Pharma industry highly preferred

Options

Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
Share on your newsfeed

Tell Us About Yourself

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