Covance

  • GLP Quality Assurance Manager , BioAnalytical Labs

    Job Location(s) US-UT-Salt Lake City
    Job Number
    2017-14574
    Job Category
    Quality Assurance
    Position Type
    Full-Time
  • 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 will be based at the Salt Lake City, UT Covance location.

     

     

    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 current regulatory 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 current regulatory 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

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