Covance GLP Quality Assurance Manager , BioAnalytical Labs in Salt Lake City, Utah

Job Overview

Covance Manager, Quality Assurance

Apply your leadership experience at a global company

Are you leader known for building effective working relationships? Can you ensure 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 our quality assurance teams, consider joining Covance as a Manager in our Bioanalytical Quality Assurance group. In this role, you will lead, manage and coach a QA team ensuring compliance to quality standards through the performance of project, process-based, and facility inspections as you:

  • Audit bio-analytical (LC/MS-MS) data and technical reports

  • Act as the primary contact for clients and regulatory inspections and as the site expert for regulatory guidelines

  • Provide training to technical and professional staff on GLP regulations

  • Lead ongoing process improvements to improve best practices

  • Instill and manage a culture of continuous improvement, quality, and productivity

  • Participate in outside agency or sponsor related inspections or inquiries, as required

This position can be based out of any of the following Covance locations: Salt Lake City, UT; Chantilly, VA; Greenfield, IN; Indianapolis, IN; Madison, WI; or Princeton, NJ. Some travel is required.

Working and thriving at Covance

As part of the global QA leadership 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 take care of you with 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 Assurance Managers 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 supportive 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 5 years of experience in a GLP/GCP regulated environment with at least 2 years of demonstrated leadership experience

  • Advanced working knowledge of currentregulatory guidelines including GLP and 21 CFR Part 11 and a general knowledge of ICH GCP compliance

  • Working knowledge of FDA Guidance for Industry, Bioanalytical Method Validation (LC/MS-MS preferred) , and experience with Watson LIMs and Analyst software preferred

  • 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 Manager in Quality Assurance, 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 and nurture 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 5 years of experience in a GLP/GCP regulated environment with at least 2 years of demonstrated leadership experience

  • Advanced working knowledge of currentregulatory guidelines including GLP and 21 CFR Part 11 and a general knowledge of ICH GCP compliance

  • Working knowledge of FDA Guidance for Industry, Bioanalytical Method Validation (LC/MS-MS preferred), and experience with Watson LIMs and Analyst software preferred

  • 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

Job Number 2017-14574

Job Category Quality Assurance

Position Type Full-Time

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.