• Analytical GMP Strategy & Compliance Leader…

    Lilly (Lebanon, IN)
    …implement the necessary systems and business processes required to support GMP operations. This will require significant collaboration, creativity and resilience as ... goes from design, to start-up, and to steady-state operations. The Analytical GMP Strategy & Compliance Director role, a technical-track position, seeks a… more
    Lilly (08/08/25)
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  • Director, Global Quality & Compliance Support

    Merck (Indianapolis, IN)
    …are seeking a dynamic and experienced Quality & Compliance Director to lead GMP compliance across our global network of internal and external contract manufacturing ... (APIs) and finished products, including biologics and vaccines. As a trusted GMP compliance expert, you will drive regulatory excellence, support health authority… more
    Merck (08/08/25)
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  • Associate Director, Plant Engineering - Lilly…

    Lilly (Lebanon, IN)
    …and implement the necessary systems and business processes required to support GMP operations, and build the site culture. This will require significant ... collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing through start up. Key Responsibilities: + Responsible for oversight of… more
    Lilly (08/08/25)
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  • HVAC Engineer

    Lilly (Indianapolis, IN)
    …impact. The HVAC Engineer is the site Subject Matter Expert (SME) for site HVAC ( GMP and non GMP ) and the ancillary systems associated within the facilities. ... responsible for effectively, reliably, and cost effectively operating the site's HVAC ( GMP and non- GMP ) and ancillary systems associated within the facilities,… more
    Lilly (08/02/25)
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  • Principal Specialist, Quality Assurance

    Cardinal Health (Indianapolis, IN)
    …for raw material, work in process, and finished products. + Champion Quality, GMP compliance and EHS/Radiation Safety practices. + Develop and lead GMP /GDP ... outcomes. + Able to challenge, appropriately, the design, conduct, and reporting of GMP activities including metrics and annual reporting. In that context, has the… more
    Cardinal Health (08/09/25)
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  • Sr. Director - Quality Control

    Lilly (Lebanon, IN)
    …to build the processes and facility to enable a successful startup into GMP manufacturing operations._ **Main Purpose and Objectives:** The Senior Director - Quality ... and implementing the necessary systems and business processes required to support GMP operations, and building the site culture. This will require significant… more
    Lilly (06/21/25)
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  • Director, Microbiology

    Bristol Myers Squibb (Indianapolis, IN)
    …the day-to-day activities to support clean room environmental monitoring, GMP testing and release of radiopharmaceutical drug substances/products. The Director, ... Develop KPI's to ensure operational excellence and compliance with GMP 's. + Manage laboratory operations budget and forecast. +...+ A minimum of 10 years of experience in GMP microbiological testing or environmental monitoring to support aseptic… more
    Bristol Myers Squibb (08/10/25)
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  • Sr. Manufacturing Operations Associate

    Lilly (Lebanon, IN)
    …to build the processes and facility to enable a successful startup into GMP manufacturing operations. The Manufacturing Operations Associate (OA) for the Lilly API ... implementing new technologies and operational process improvements in the GMP manufacturing environment. **As a Manufacturing Operations Associate, your… more
    Lilly (08/08/25)
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  • Maintenance & Calibration Technician

    PDS Tech Commercial, Inc. (Indianapolis, IN)
    …detail-oriented **Maintenance & Calibration Technician** to support a state-of-the-art GMP Radioligand Therapies production facility in Indianapolis, IN. If you're ... calibration, and maintenance of sophisticated equipment and systems supporting GMP manufacturing. From cleanroom production lines to building utilities and… more
    PDS Tech Commercial, Inc. (08/07/25)
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  • Quality Control Scientist - Weekend Night Shift

    Novo Nordisk (Bloomington, IN)
    …maintenance and basic laboratory maintenance activities while maintaining a GMP quality system. Other duties will include data review/archiving, database ... at least 3 years of experience, including 1 year GMP experience or regulated industry, required OR + Master's...up to 2 years of experience, including 1 year GMP experience regulated industry, required OR + PhD in… more
    Novo Nordisk (08/02/25)
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