• Sr . Director - Global Patient Safety…

    Lilly (Indianapolis, IN)
    …life better for people around the world. **Purpose:** The purpose of the Senior Director - Signal Management Group Leader, is to provide strategic leadership for ... end-to-end Signal Management Processes and associated metrics throughout the product lifecycle ensuring signal detection, evaluation and management processes meet… more
    Lilly (08/22/25)
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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 (09/05/25)
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  • Senior Principle Scientist

    Merck (Indianapolis, IN)
    …Liaison provides strategic regulatory oversight to accelerate approvals and optimize product labeling. This position requires an experienced leader who is proactive, ... + Serve as an experienced worldwide regulatory representative on Asset or Product Development Teams and act as the regulatory single point-of-contact for assigned… more
    Merck (08/23/25)
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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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  • Clinical Research Scientist , Medical…

    Lilly (Indianapolis, IN)
    …new product development activities over the entire spectrum of drug development and clinical trial phases. Specific activities include developing or contributing ... the application of scientific and clinical training and expertise, the Clinical Research Scientist (CRS) is an integral member of the medical affairs, development or… more
    Lilly (09/05/25)
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  • Scientist - Lab Informatics, LabVantage…

    Lilly (Indianapolis, IN)
    …to make life better for people around the world. **Responsibilities:** + The Sr . Principal Associate - Lab Informatics -LabVantage LIMS/LES Program is part of a ... with LIMS/LES such as other manufacturing and automation systems. + The Sr . Principal Associate - Lab Informatics -LabVantage LIMS/LES Program is responsible for… more
    Lilly (08/29/25)
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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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  • Advisor/ Senior Advisor - Process Chemistry…

    Lilly (Indianapolis, IN)
    drug substance manufacturing. + 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...needs across the rapidly evolving portfolio of medicines. The scientist will collaborate with a growing team comprised of… more
    Lilly (08/20/25)
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