• Senior Advisor/Director Global Regulatory…

    Lilly (Indianapolis, IN)
    …+ Demonstrated deep technical knowledge and experience of small molecule drug product development, commercialization and manufacturing processes. + Prior ... patients who need them all over the world. The Senior Advisor/Director Post approval scientist in Global...regulatory strategies that support the lifecycle of the assigned product (s). Key responsibilities: + Deep technical knowledge of solid… more
    Lilly (09/03/25)
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  • Senior R&D Scientist

    Catalent Pharma Solutions (Greendale, IN)
    …to solve difficult development and manufacturing challenges. The Senior R&D Scientist will initiate, coordinate, and implement new product initiatives on new ... ** Senior R&D Scientist (Food Scientist...service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested… more
    Catalent Pharma Solutions (08/01/25)
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  • 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 (09/04/25)
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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 (08/30/25)
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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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  • 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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  • 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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  • 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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