• Associate Director , IDM Project…

    Lilly (Indianapolis, IN)
    …Lilly organizations + Demonstrated knowledge of manufacturing equipment, controls, and validation practices + Direct experience within a manufacturing environment + ... Awareness of GMP and ISO requirements related to medical devices and device assembly operations Additional Preferences: + Previous experience with capital project delivery, commissioning, and qualification of automated systems + Process automation experience… more
    Lilly (04/24/25)
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  • Director , Production

    Bristol Myers Squibb (Indianapolis, IN)
    …team, RayzeBio aims to be the global leader in radiopharmaceuticals. The Director , Production is an integral part of bringing RayzeBio's innovative drug products ... patients in need. In this role, you will report directly to the Director , Operations and be primarily responsible for directing the day-to-day production activities… more
    Bristol Myers Squibb (05/27/25)
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  • Manufacturing Operations Associate

    Lilly (Lebanon, IN)
    …+ When required (and per delegation procedure), in the absence of the Associate Director -Manufacturing provide continuity to the Process Team activities and ... a successful startup into GMP manufacturing operations. The Manufacturing Operations Associate (OA) for the Lilly API Manufacturing Facility (LP1), Lebanon, Indiana,… more
    Lilly (05/09/25)
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  • Sr. Manager - Device Assembly & Packaging…

    Lilly (Indianapolis, IN)
    …through involvement in teams as directed by the Manager. Partners with Operations Associate Director for business planning. **Minimum Requirements:** + 3-5 years ... leadership informed of issues. Coordination with maintenance, engineering, automation, validation and technical services on projects is critical to success.… more
    Lilly (05/20/25)
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  • QA Scientist - Quality Operations

    Lilly (Indianapolis, IN)
    …coach operations and support personnel on quality matters. + Effectively communicate with Associate Director - QA and other Quality Representatives on quality ... met (ie, deviations / observations, procedures, specifications, technical studies, validation protocols, change controls, CAPA, engineering documents, etc.). +… more
    Lilly (03/14/25)
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