• Specialist II, Formulation / Filling Tues.-Fri., 6…

    Novo Nordisk (Bloomington, IN)
    …Product - Secondary + Perform Manufacturing review of all types of GMP Documentation including Master Batch Records, Engineering Studies, Logbooks, Forms, etc. to ... required + 5 years pharmaceutical and/or manufacturing experience required + 5 years GMP experience + Technical Requirements + Proficient in Excel, Word, and other… more
    Novo Nordisk (07/23/25)
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  • Slitter Operator

    WestRock Company (Knox, IN)
    …compliance of all GMPs. * Maintain housekeeping excellence in accordance with NSF/ GMP Housekeeping standards. * Follow all safety procedures and promote safety & ... departmental quality checks. Participate and ensure department is compliant with NSF/ GMP audit regulations. * Ability to safely operate various manufacturing… more
    WestRock Company (07/22/25)
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  • Operator III, Inspection Sun-Fri 11 PM-7:30 AM

    Novo Nordisk (Bloomington, IN)
    …maintaining visual factory + Required to read, understand, follow, and review GMP documents + Leads area continuous improvement activities + Reports safety, quality ... + 3 years of direct pharmaceutical manufacturing experience + 3 years of GMP experience + Technical Requirements + Proficient with Microsoft Office programs, Email,… more
    Novo Nordisk (07/18/25)
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  • Sanitor - Night Shift -Bakery Plant

    Conagra (Indianapolis, IN)
    …Follow and comply with all Safe Quality Food (SQF) and Good Manufacturing Practices ( GMP 's). + Use hand tools to change process flow piping and prepare sanitation ... (with PLCs or MMIs) + Experience work in a USDA, FDA, OSHA, or GMP compliant environment + Proficiency in MS Office Programs + Proficiency in SAP **ESSENTIAL… more
    Conagra (07/18/25)
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  • Lead, Inspection Sun-Fri 11 PM - 7:30 AM

    Novo Nordisk (Bloomington, IN)
    …+ Escalate behavioral or non-conformance to Supervisor + Advance Documentation Skills ( GMP preferred) + Capable of working with minimal supervisor and high-level ... + 2 years of direct pharmaceutical manufacturing experience + 2 years of GMP experience + Technical Requirements + Proficient in Excel, Word, and other office… more
    Novo Nordisk (07/18/25)
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  • Technical Supervisor

    Primo Brands (Indianapolis, IN)
    …to internal and external regulations, procedures & policies + Maintain cleanliness to GMP standards and ensure all safety standards are met * + Effectively ... food or other clean manufacturing environment with familiarity with quality, GMP and hygiene regulations preferred. + Prior experience with pneumatics, hydraulics,… more
    Primo Brands (07/18/25)
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  • Forklift Operator - Receiving - Bakery Plant 3rd…

    Conagra (Indianapolis, IN)
    …Follow and comply with all Safe Quality Food (SQF) and Good Manufacturing Practices ( GMP 's). + Pick up and remove waste from production line floors and containers. ... or packaging environment + Experience work in a USDA, FDA, OSHA, or GMP compliant environment **ESSENTIAL PHYSICAL AND MENTAL REQUIREMENTS:** + Sit, stand, walk and… more
    Conagra (07/16/25)
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  • Principal Associate - Environmental LDAR - Lebanon…

    Lilly (Lebanon, IN)
    …to build the processes and facility to enable a successful startup into GMP manufacturing operations. **Job Position Overview:** The Principal Associate - LDAR is ... collaboration, creativity, and resilience as the site grows to full-scale GMP manufacturing. **Responsibilities:** + Oversee a team of LDAR technicians, providing… more
    Lilly (07/11/25)
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  • Engineer - Process - Formulation

    Novo Nordisk (Bloomington, IN)
    …team, including operational protocol development, to implement compliance with FDA GMP requirements + Identify improvements and efficiencies of facility preventative ... the degree required + A minimum of 2 years of experience working in a GMP environment in the pharmaceutical or medical device industry is required; 5 years of… more
    Novo Nordisk (07/10/25)
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  • Advisor - Electronic Lab Systems (LabVantage LIMS…

    Lilly (Indianapolis, IN)
    …requirements for eLAB systems. + Prepares, reviews, and approves GMP documentation (eg, Non-Conformances, Procedures, Protocols, Specifications, and Change Controls) ... validation, and compliance within regulated environments. + Experience supporting GMP manufacturing or quality laboratories, preferably related to APIs or… more
    Lilly (07/09/25)
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