• Director, IT Applications

    Sumitomo Pharma (Indianapolis, IN)
    …to **GXP, FDA, and other regulatory requirements** applicable to the pharmaceutical industry, including validation and documentation standards. **Team Management ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in...as the key interface between the IT department, Business Process Owners, and Executive Leadership. **Qualifications** + **15+ years… more
    Sumitomo Pharma (12/23/25)
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  • Associate Director, IT Compliance & Governance

    Sumitomo Pharma (Indianapolis, IN)
    Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the US (Sumitomo Pharma America, Inc.), focused on addressing patient ... **Job Overview** Lead IT compliance and governance programs in a regulated pharmaceutical environment. Ensure adherence to global regulations (GxP, FDA, EMA), manage… more
    Sumitomo Pharma (01/10/26)
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  • Engineer - MES System

    Lilly (Indianapolis, IN)
    …experience. + **Additional Information:** + Experience maintaining Computer Systems Validation in line with pharmaceutical computer system quality ... with cross-functional subject matter experts, working to understand the manufacturing process and translate them into system requirements. You will take these… more
    Lilly (01/20/26)
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  • Advisor - Data Strategy and Orchestration - Lilly…

    Lilly (Lebanon, IN)
    …and methodologies that position the Medicine Foundry as a leader in pharmaceutical data management. This role will develop novel approaches to data infrastructure, ... advance the state-of-the-art in pharmaceutical data technologies, and apply deep technical expertise to solve complex data challenges across the digital plant… more
    Lilly (01/09/26)
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  • Director/Senior Director, Global Process

    Lilly (Indianapolis, IN)
    …across the network. **Position Brand Description:** The Director/Senior Director, Global Process Owner for Sterility Assurance, as a leader within the Technical ... and maintain the global quality system procedural requirements for a Level 2 Process related to Aseptic Processing controls inclusive of Aseptic Process more
    Lilly (10/24/25)
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  • Principal Process Engineer

    Lilly (Indianapolis, IN)
    …being flexible, proactive and involved. Serve as a responsible engineer for site process lines by possessing a deep knowledge of equipment and unit operation design ... impact on the safety or quality integrity of the equipment or process . **Innovation and Problem-Solving:** + Provide equipment and processing support for production… more
    Lilly (12/11/25)
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  • Associate Director - Joint Process Team

    Lilly (Indianapolis, IN)
    Process Research & Development group on commercialization (technology transfer, process validation and regulatory approval) of Lilly's exciting leading ... life better for people around the world. The Associated Director of the Joint Process Team (JPT) is responsible for leading a cross functional team comprised of both… more
    Lilly (11/15/25)
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  • Associate Director - Joint Process Team

    Lilly (Indianapolis, IN)
    Process Research & Development group on commercialization (technology transfer, process validation and regulatory approval) of Lilly's exciting leading ... through philanthropy and volunteerism. **Outline of Role:** Associate Director, Joint Process Team (JPT) is responsible for leading a cross functional team… more
    Lilly (12/18/25)
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  • Director, Analytical Chemistry - Antibody-Drug…

    Lilly (Indianapolis, IN)
    …Located in Indianapolis, IN, scientists have full access to Lilly's deep pharmaceutical development expertise and engineering capabilities. In this role, we are ... apply their strong foundation in analytical sciences and experience in pharmaceutical development to enable clinical trials, regulatory submissions, and new product… more
    Lilly (12/15/25)
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  • IDAP Engineer - MES Systems

    Lilly (Indianapolis, IN)
    …assembly or packaging operations. + Working knowledge of cGMP and Computer System Validation (CSV) frameworks + Ability to interpret process requirements and ... and validation . + 3+ years of experience in regulated pharmaceutical or medical device manufacturing environments. **Additional Preferences:** + Familiarity with… more
    Lilly (01/09/26)
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