• BL1 Utility 1st Shift - Bakery

    Conagra Brands (Indianapolis, IN)
    …follow and comply with all Safe Quality Food (SQF) and Good Manufacturing Practices ( GMP 's). + You maintain mastery on all skills that the associate has been ... perform other tasks that the Team Leader or Line Lead might require. + You work overtime to achieve...environment + work in a USDA, FDA, OSHA, or GMP compliant environment **ESSENTIAL PHYSICAL AND MENTAL REQUIREMENTS:** +… more
    Conagra Brands (10/29/25)
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  • IT&D Associate Manager, Smart Mfg. + S&O

    Reckitt (Evansville, IN)
    …hands-on experience in IT infrastructure and operational technology. **Your responsibilities** + Lead all IT&D activities at the site, ensuring alignment with both ... equipment interfaces. + Drive site-level compliance with cybersecurity standards, GMP /GxP requirements, and audit readiness. + Manage stakeholder communications and… more
    Reckitt (11/18/25)
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  • Process Scientist - TS/MS Lab - Lebanon API…

    Lilly (Lebanon, IN)
    …the facility and the culture to enable a successful startup into GMP manufacturing operations. **Main Purpose and Objectives:** Lilly is seeking a process ... + Effective management of multiple projects. + Utilizes technical skills to lead or perform in-depth investigations for out of specification results and aberrant… more
    Lilly (11/12/25)
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  • Analytical Scientist - TS/MS Lab - Lebanon API…

    Lilly (Lebanon, IN)
    …build the processes and facility to enable a successful startup into GMP manufacturing operations. **Main Purpose and Objectives:** The TS/MS Analytical Scientist is ... Accurately record data in accordance with TSMS laboratory procedures, standards, and GMP requirements. + Adhere to all Environmental, Health, and Safety standards. +… more
    Lilly (11/12/25)
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  • Analytical Technical Steward Peptides…

    Lilly (Indianapolis, IN)
    …validation, and reference standard characterization. + Utilizes technical skills to lead or perform in-depth investigations for out of specification results and ... 5+ years of industry related experience in pharmaceuticals in a GMP lab (Large Molecule, Peptide, and/or Oligonucleotide strongly preferred) **Additional… more
    Lilly (11/01/25)
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  • Production Supervisor

    Nestle (Anderson, IN)
    …assigned area. Your role spans financial performance, employee safety, and team development. You lead and manage a shift of 20-60 employees, taking an active role in ... objectives are met including regular adherence to Good Manufacturing Practices ( GMP 's), performance of sanitation audits, food safety checks, and product quality… more
    Nestle (10/30/25)
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  • Associate Director - Engineering API External…

    Lilly (Indianapolis, IN)
    …Peptides and Large Molecule is a member of the API EM Plant Lead Teams providing leadership and expertise to reliably supply and commercialize externally ... Large Molecule as a member of the APIEM Plant Lead Team, HSE Lead Team, Science ...or indirect experience with commercialization (Validation, Tech Transfer, CMC, GMP , Quality, and/or HSE) + Demonstrated ability to function… more
    Lilly (09/26/25)
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  • Associate Director - TS/MS Device & Packaging

    Lilly (Indianapolis, IN)
    …Science (TS/MS) in the Device and Packaging Network, you will lead the charge in ensuring operational excellence and driving technical innovation ... control and capability. **Key Objectives and Deliverables:** Empowerment through Development: Lead , mentor, coach, and develop staff, fostering a culture of… more
    Lilly (09/12/25)
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  • Advisor/Senior Advisor Downstream Purification…

    Lilly (Indianapolis, IN)
    …to solve problems and benchmark potential solutions. **Responsibilities:** + Lead the design, execution and interpretation of appropriate purification development ... physical and chemical processing conditions on recombinant protein product quality. + Lead the development of validated scaled-down models of key bioprocess unit… more
    Lilly (11/14/25)
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  • Operations Supervisor (Indy RLT)

    Lilly (Indianapolis, IN)
    …Indy RLT is responsible for shift leadership of manufacturing employees. They will lead the production of drug products following strict cGMP guidelines and are ... finished dosage form (FDF) drug products and radioisotope products. + Lead investigation, resolution, and mitigation of deviations, non-conformances, and OOS (Out… more
    Lilly (11/21/25)
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