• Associate Director

    Bristol Myers Squibb (Indianapolis, IN)
    …entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals . The Associate Director of Validation is responsible for leading the ... and company standards for pharmaceutical/radiopharmaceutical production. This role oversees validation activities from initial planning through execution, manages a… more
    Bristol Myers Squibb (11/26/25)
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  • Associate Director - Joint Process…

    Lilly (Indianapolis, IN)
    …Lilly and Active Pharmaceutical Ingredient (API) Contract Manufacturer representatives. The JPT Associate Director is the key business relationship owner and is ... materials are delivered on time and within downstream customer expectations. The JPT Associate Director will partner with Lilly's Process Research & Development… more
    Lilly (11/15/25)
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  • Associate Director - TS/MS Peptides

    Lilly (Indianapolis, IN)
    …world. Eli Lilly and Company is seeking an experienced and highly motivated Associate Director to join our Technical Services/Manufacturing Science (TS/MS) team, ... peptide processes from development to manufacturing, ensuring successful scale-up, validation , and regulatory compliance. * Design, execute, and interpret… more
    Lilly (11/13/25)
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  • Associate Director - TS/MS Device…

    Lilly (Indianapolis, IN)
    …as we achieve drug product manufacturing and commercialization excellence. As the Associate Director of Technical Services/Manufacturing Science (TS/MS) in the ... procedures, deviation investigations, technical reports, change controls, regulatory submissions, validation protocols and summary reports, PFDs, APRs, etc. +… more
    Lilly (09/12/25)
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  • Associate Director - Engineering

    Lilly (Indianapolis, IN)
    …lead the charge in shaping the future of manufacturing at Eli Lilly? As an Associate Director of Engineering, you'll be at the forefront of this exciting ... procedures, deviation investigations, technical reports, change controls, regulatory submissions, validation protocols and summary reports, PFDs, APRs, etc. 4.… more
    Lilly (09/11/25)
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  • Associate Director - TS/MS - Lebanon…

    Lilly (Lebanon, IN)
    …a successful startup into GMP manufacturing operations._ **Position Description:** The Associate Director - Technical Services/Manufacturing Science (TSMS) is ... responsible for managing the activities of TSMS personnel. The Associate Director TSMS must balance coaching a technical staff, prioritization and staffing for… more
    Lilly (10/14/25)
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  • Associate Director , Small Molecule…

    Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
    ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... drug product at CDMOs + Design and lead method validation and implementation activities for drug substance and drug product ensuring compliance with relevant ICH and… more
    Otsuka America Pharmaceutical Inc. (11/25/25)
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  • Associate Director - Engineering API…

    Lilly (Indianapolis, IN)
    …solutions to support communities through philanthropy and volunteerism. **Responsibilities:** The Associate Director - API EM Engineering Leader for Peptides ... processes, and functions. + Direct or indirect experience with commercialization ( Validation , Tech Transfer, CMC, GMP, Quality, and/or HSE) + Demonstrated ability… more
    Lilly (09/26/25)
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  • Associate Director , IT Regulatory,…

    Bristol Myers Squibb (Indianapolis, IN)
    …aims to be the global leader in radiopharmaceuticals. **Job Description** The Assoc. Director , IT Regulatory, Clinical and Enterprise Systems is an integral part of ... patients in need. In this role, you will report directly to the Exec. Director , IT and be primarily responsible for implementing RayzeBio's vision for growth and… more
    Bristol Myers Squibb (11/22/25)
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  • Associate Director - Drug Product…

    Lilly (Indianapolis, IN)
    …with CMs to ensure alignment of intents and objectives. + Validation : ensure proper definition of strategies, revisions, protocol approvals, validation ... External Manufacturing documentation (eg, Quality Agreements, Manufacturing Requirements Document, validation documents) is in place and in compliance. + Build… more
    Lilly (11/22/25)
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