• Laboratory Information Management System (LIMS) Administrator

    Posting Date 4 months ago(3/19/2019 9:28 AM)
    Requisition ID
    Job Location(s)
    Pittsburgh PA United States
    Position Type
    Full Time
    Cook Myosite Inc.
    Information Technology
  • Overview

    Cook MyoSite, Inc. is on a mission to make regenerative medicine a part of everyday medicine. We’re investigating our core technology, autologous muscle-derived cells, for the potential treatment of several muscle-related disorders. We at Cook MyoSite have the potential to make a difference in the lives of countless people around the world, and we also have the potential to make a difference in yours. Joining our team is an opportunity to ignite your passion, grow your potential, and define your purpose. If you’re curious, motivated by helping others, and driven by integrity, we invite you to apply below.


    The Laboratory Information Management System (LIMS) Administrator at Cook Myosite Inc. will design, configure, customize and write programming code to support the development and maintenance of the LIMS.


    • Work as a member of the applications development and administration team to maintain and enhance the functionality of the LIMS
    • Perform system configuration and customization using standard suite of tools
    • Create custom code to automate LIMS system processes

    • Perform troubleshooting and analysis
    • Participate in requirements elicitation meetings
    • Lead software demonstrations to ensure that end-user requirements are met
    • Perform end-user training
    • Document system design characteristics


    • Bachelor’s degree in a Computer Systems related discipline, Life sciences, Engineering or Business; or consummate  experience to provide a comparable background
    • 2+ years related experience in LIMS development and administration
    • Workflow development, documentation and translation to automated systemsProficient in LIMS BASIC and SQL languages, and relational database development
    • Experience with creating custom Crystal Reports is a plus
    • Life Science background preferred
    • Experience working with ISPE GAMP 5 and GxP is a plus
    • Basic understanding of cGMP, 21 CFR Part 11, and related regulations associated with Bio/Pharmaceutical product manufacturing
    • Effective written and verbal communication
    • Able to work well with, and understand the needs of, end users, system owners, managers, quality and software developers
    • Experience developing solutions in LabWare ELN is a plus
    • Experience in instrument integration/automation within LIMS is a plus



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