• Senior Data Scientist , Specialist…

    Deloitte (Indianapolis, IN)
    Senior Data Scientist , Specialist Senior - SFL Scientific Our Deloitte Strategy & Transactions team helps guide clients through their most critical moments ... in building industry-specific, artificial intelligence (AI) technologies. We are hiring a Senior Data Scientist to collaborate directly with clients to design… more
    Deloitte (06/05/25)
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  • Senior Principal Scientist /Advisor,…

    Lilly (Lebanon, IN)
    …a successful startup into GMP manufacturing operations. **Position Description** The Senior Principal Scientist /Advisor, MES will support implementation of ... MES platform within the Lilly Lebanon API site. **Key Objectives/Deliverables** The Senior Principal Scientist /Advisor, MES will represent the TS/MS function in… more
    Lilly (05/21/25)
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  • Senior Principal Scientist

    Lilly (Indianapolis, IN)
    …establish starting material rationales, identify impurities, and coordinate the testing of drug substance / drug product quality characteristics. + Provide ... the next generation of life-changing medicines to patients. **Position Summary:** The Senior Principal Scientist , Analytical Chemistry, will join a diverse team… more
    Lilly (05/31/25)
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  • Advisor Research Scientist (Purification)…

    Lilly (Indianapolis, IN)
    …the value chain and in multiple locations + Understanding the interaction of bulk drug substance and drug product formulationinteraction of equipment set(s) ... process control, yield, purity and/or productivity. + The Research Scientist / Senior Research Scientist should also...with process ( drug substance and drug product ) + Significant experience with registration,… more
    Lilly (06/09/25)
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  • Clinical Research Scientist , Medical…

    Lilly (Indianapolis, IN)
    …around the world. The primary responsibilities of the Development Clinical Research Scientist are generally related to late-phase and marketed compounds. The core ... that addresses key customer needs (patient, provider, and payer); the product lifecycle plan, clinical strategies, development plans and study protocol design.… more
    Lilly (08/01/25)
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  • Scientific Director/ Sr

    Lilly (Indianapolis, IN)
    …clinical and commercial settings. + Collaborate across internal CMC networks ( Drug Product Delivery, Project Management, Quality, Manufacturing, and Regulatory) ... Development (SMDD) is responsible for the development of synthetic drug substances and drug products from the...the rapidly evolving Lilly Genetic Medicines (LGM) portfolio. The scientist will collaborate with a growing team comprised of… more
    Lilly (07/22/25)
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  • Principal Scientist , TSMS Cleaning…

    Lilly (Indianapolis, IN)
    …communities through philanthropy and volunteerism. **Position Brand Description:** The Lilly API/Dry Product Network is rapidly expanding to meet the demand for new ... respective functions but will be coordinated by the Ramp Team Sr . Director. **Key Objectives/Deliverables** **:** Responsible for the development, implementation and… more
    Lilly (07/29/25)
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  • Advisor/ Senior Advisor Global Regulatory…

    Lilly (Indianapolis, IN)
    …to patients who need them all over the world. The Advisor Post approval scientist in Global Regulatory Affairs - CMC Commercial Products will leverage CMC technical ... regulatory strategies and submissions for Lilly's commercial products. The regulatory scientist will be expected to demonstrate innovative regulatory strategies that… more
    Lilly (07/22/25)
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  • Senior Director - GPS Benefit-Risk…

    Lilly (Indianapolis, IN)
    …make life better for people around the world. **Purpose:** The purpose of the Senior Director - Benefit-Risk Management Group Leader is to lead the development and ... Lilly's end-to-end benefit-risk management processes and associated metrics throughout the product lifecycle. This role will also spearhead the redesign and… more
    Lilly (06/25/25)
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  • Senior Advisor/Director, Global Regulatory…

    Lilly (Indianapolis, IN)
    …of evolving regulatory initiatives desirable. + Relevant experience in synthetic molecule drug substance and/or drug product development, commercialization, ... new medicines to patients who need them all over the world. The Senior Advisor/Director in Global Regulatory Affairs - CMC Pre-approval Small Molecules will leverage… more
    Lilly (07/02/25)
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