• Sr. Associate - QA - API

    Lilly (Indianapolis, IN)
    …QAAPI or finished product manufacturing **Additional Preferences:** + Previous GMP manufacturing knowledge + Thorough technical understanding of quality ... activities including batch disposition of API batches at Contract Manufacturing organizations (CMs). The Associate - QA...batches at Contract Manufacturing organizations (CMs). The Associate - QA - API's position is essential for… more
    Lilly (06/03/25)
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  • Associate Director- Idap MES Architect…

    Lilly (Indianapolis, IN)
    …Bring:** + Proven experience implementing and architecting MES solutions in GMP -regulated manufacturing environments. + Deep technical knowledge of PharmaSuite ... are determined to make life better for people around the world. As the Associate Director of Tech@Lilly for the Indianapolis Device Assembly & Packaging (IDAP) site,… more
    Lilly (05/30/25)
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  • MQA Associate

    Actalent (Portage, IN)
    Job Title: MQA AssociateJob Description We are seeking an MQA Quality Associate to join our team on the 2nd shift. This role involves assisting with AQL testing, ... and other production support duties. + Monitor all operations related to manufacturing to ensure adherence to AQST policies and procedures. + Conduct routine… more
    Actalent (05/28/25)
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  • Food Production Associate

    Staff Management | SMX (Indianapolis, IN)
    …Maintains a safe and clean environment by adhering to safety policy and Good Manufacturing Practices ( GMP ) procedures. + May assist with cleaning and sanitation ... part of our production team, you will be responsible for several different manufacturing activities. You will be working in a fast-paced manufacturing … more
    Staff Management | SMX (06/02/25)
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  • Associate Director - Warehouse Operations…

    Lilly (Indianapolis, IN)
    …to create the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research ... and manufacturing in a single location, the Medicine Foundry will...also reducing costs and environmental impact. **Position Description:** The Associate Director-Warehouse Operations will be engaged in the delivery… more
    Lilly (06/06/25)
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  • Associate /Sr. Associate - QA API

    Lilly (Indianapolis, IN)
    …Operations manufacturing and laboratories and ensures quality systems and GMP compliance. The QA Representative provides assistance and guidance in deviation ... who are determined to make life better for people around the world. **Position Brand Description:** The Associate - QA - IAPI provides support to Indianapolis API… more
    Lilly (05/15/25)
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  • Associate Director Device TS/MS Product…

    Lilly (Indianapolis, IN)
    …+ Knowledge of pharma and/or combination product manufacturing (ideally discrete manufacturing ) + Understanding of GMP and ISO requirements for Combination ... for people around the world. **Organization Overview:** The Indianapolis Device Manufacturing site provides ownership and oversight of the Lilly Commercial Device… more
    Lilly (05/14/25)
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  • Associate Director - Device…

    Lilly (Indianapolis, IN)
    …combination product commercialization actives through mid- to late-stage development into manufacturing readiness and commercial launch. The role reports into the ... Indianapolis Device Manufacturing (IDM) organization, and is responsible for the successful...device / combination product quality & regulatory requirements, including GMP /CFR, EU MDR, ISO and IEC requirements + Familiarity… more
    Lilly (05/28/25)
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  • Associate Director - Operations

    Lilly (Indianapolis, IN)
    …Brand Description:** Are you ready to lead the charge in shaping the future of manufacturing at Eli Lilly? As an Associate Director of Operations, you'll be at ... innovation, foster growth, and make a meaningful impact within the manufacturing landscape at Eli Lilly! **Key Objectives/Deliverables:** + **Empowerment through… more
    Lilly (06/05/25)
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  • Sr. HSE Associate

    Lilly (Indianapolis, IN)
    …significant collaboration and resilience as the site grows through startup to full scale GMP manufacturing . Post start-up, this role will continue to be the ... the necessary systems and business processes required to support GMP operations, and build the site safety culture. This...programs and serve as an HSE regulatory advisor for manufacturing and support units. **Key Responsibilities:** + Assist with… more
    Lilly (03/17/25)
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