• Engineer - Automation

    Lilly (Indianapolis, IN)
    process automation engineer or process engineer is desirable. + Pharmaceutical experience is desirable. + Computer System Validation experience is ... either strategic or tactical concerning business needs. Ensure that process automation solutions/systems are in-control, capable, and compliant. **Responsibilities:**… more
    Lilly (05/10/25)
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  • Senior Manager, IT - Digital Plant Applications…

    Bristol Myers Squibb (Indianapolis, IN)
    …ensure the digital systems applications along with CSV for lab and process automation are enabled and maintained to successfully deliver novel Radiopharmaceutical ... technologies. You will work with lab & process automation, large corporate systems, small biotech systems, across all functions for the Indianapolis site(s).… more
    Bristol Myers Squibb (05/11/25)
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  • Engineer - Warehouse

    Lilly (Indianapolis, IN)
    …on projects associated with regulatory compliance, commercialization, capacity, and process improvement efforts. This specific role will be responsible for ... project delivery, this role will become a member of the warehouse process team, providing engineering support to the warehouse areas during production operations.… more
    Lilly (05/06/25)
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  • Senior Corporate Compliance Specialist - Medical…

    Fujifilm (Indianapolis, IN)
    …of action plans, and prepare related reports. + Manage transparency data collection, validation , and reporting process to ensure compliance with the applicable ... teams and provide guidance on questions related to compliance program, process , and requirements. Understand and support business strategy and collaborate with… more
    Fujifilm (05/21/25)
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  • Associate Director - Infrastructure Lead

    Lilly (Lebanon, IN)
    …of experience in a related field.. **Additional Preferences** + Experience in Pharmaceutical GMP Manufacturing + Experience supporting Process Automation systems ... improve business value. + Critically evaluate user requests, using technical and process knowledge to determine + underlying business needs. + Provide leadership and… more
    Lilly (05/01/25)
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  • QA Scientist - Quality Operations

    Lilly (Indianapolis, IN)
    …met (ie, deviations / observations, procedures, specifications, technical studies, validation protocols, change controls, CAPA, engineering documents, etc.). + ... triage deviations / observations that occur within the local process team. + Lead, mentor, and coach operations and...a STEM field + 3+ years working in the pharmaceutical manufacturing industry, preferably in Quality Assurance roles **Additional… more
    Lilly (03/14/25)
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  • Engineer - Plant Engineering and Facilities

    Lilly (Indianapolis, IN)
    …to enhance equipment performance and availability + SME on flow charts, process parameters, and Engineering Function Standards + Perform process monitoring ... project to completion (scope development, budget, construction, commissioning, qualification, and validation ) + People Development: + Technical leader and mentor for… more
    Lilly (05/21/25)
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  • Rebate Analyst

    Prime Therapeutics (Indianapolis, IN)
    …The Rebate Analyst is responsible for interpreting small to intermediate pharmaceutical manufacturer contracts. This includes all aspects of the contract from ... up for each rebate period + Assist with the coordination, analysis and validation of quarterly rebate reports and distribution of quarterly invoices + Assess,… more
    Prime Therapeutics (05/19/25)
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  • Sr. Manufacturing System Administrator/Automation…

    Lilly (Lebanon, IN)
    …constructing an advanced manufacturing facility for production of API (Active Pharmaceutical Ingredient) molecules located in Lebanon, IN. This facility is Lilly's ... and administer Platform Operation and Support SOP. + Support Platform/Systems Validation activities (IQ, OQ). **Basic Requirements:** + BS in Engineering, Computer… more
    Lilly (04/19/25)
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  • Engineer-Robotics Program

    Lilly (Indianapolis, IN)
    …as Rockwell Automation Studio5000, FactoryTalk SE. + Experience in pharmaceutical manufacturing, parenteral, and/or packaging processes. + Experience in ... Commissioning & Qualification, asset delivery, validation activities, and cGMP regulations. + Knowledge in Fanuc...to request an accommodation as part of the application process and any other correspondence will not receive a… more
    Lilly (05/18/25)
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