Pace Analytical

  • Document Control Coordinator

    ID
    2018-2724
    # of Openings
    1
    Job Locations
    US-MN-Maplewood
    Category
    Science
  • Overview

    This candidate will be responsible for organizing and overseeing the review and approval of client products. This is a non-lab position.

     

    Note: This is expected to be a 6 month position.

    Responsibilities

    • Manage the review process of stability studies
    • Data entry
    • Effectively communicate updates and requirements with various stakeholders
    • Maintain Standard Operations Procedures (SOPs) for the review and approval process for all Test Methods, Work Instructions, SOPs, etc

    Qualifications

    • Bachelor’s degree in Chemistry or related science field from a four-year college or university
    • 0-1 year of experience working in a GMP laboratory
    • Basic lab techniques – notebook documentation and lab safety
    • NovaSTB and eNOVIA experience preferred
    • Good verbal and written communication skills, organization skills, and attention to detail
    • Ability to work independently or on teams and multitask

    OFCCP Statement

    Pace Analytical is an Equal Opportunity Employer and will not discriminate against any applicant for employment on the basis of race, age, religion, sex, veterans, individuals with disabilities, sexual orientation, or gender identity.

    Options

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

    Need help finding the right job?

    We can recommend jobs specifically for you! Click here to get started.