LIMS Administrator - 25-72335

Job Description:As a Lab Information Management System [LIMS] Business Administrator, you are responsible to support the maintenance and improvement of the LIMS system to Quality Operations. Maintenance support will include supporting Business Administrators in, updating master data for new and existing products, updating master data for new and existing analysis, maintaining system documentation, and providing ad hoc support to other departments. The position is expected to provide leadership to support system evolution and continuous improvement, and to support laboratory informatics needs. This role will support the creation and updating of master data to support the site transition to toa new ERP. Translation of data from existing documents to the electronic system for use in production and QC.Position Responsibilities:Ensure site on-time implementation of new iSHIFT system (ERP) activities through support of master data configuration and data migration and SOP revisions.Provide technical support of LIMS to Quality Control, Batch Release, Production, Stability and R&D operationsProvide first level diagnostic of incidents and support business users, IS LIMS Administrator and Support Center in the management and timely resolution of technicalResponsible for the master data management process including the updating of specifications and supporting the approval processManage Global System update and changes which may include new modules and workflow changesConfigure and Maintain instrument interfaces to Laboratory equipmentEnsure that the LIMS complies with all relevant regulatory standardsSupport the business in the creation and updating of training materials as changes to system occurEnsure that the LIMS complies with all relevant regulatory standardsExperience & Skills:Must have 1+ years of experience in use and administration of LabWare LIMS specifically creation of product specs, sample plans and item codes.Strong working knowledge of laboratory processes including cGMP's in a pharmaceutical environmentExperience in system testing, validation, and master data managementWorking knowledge of aseptic processes, biology, chemistry, life sciencesKnowledge of cGMPs and regulatory requirements with Strong analytical & balanced decision-making skills. Good GMP documentationFamiliar with 21CFR part 11 data integrity best practices in pharmaceutical environmentExcellent written and verbal communications skills and the ability to lead and participate in teamsExperience or familiarity of the Laboratory EnvironmentThe hourly range for roles of this nature are $50.00 to $80.00/hr. Rates are heavily dependent on skills, experience, location, and industry.

Created: 2025-06-19