• Engineer - Process - Formulation

    Novo Nordisk (Bloomington, IN)
    …team, including operational protocol development, to implement compliance with FDA GMP requirements + Identify improvements and efficiencies ... life-changing careers, and the opportunity to help improve the quality of life for millions of people around the...minimum of 2 years of experience working in a GMP environment in the pharmaceutical or medical device industry… more
    Novo Nordisk (07/10/25)
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  • BL1 Utility 1st Shift - Bakery

    Conagra (Indianapolis, IN)
    …support quality work processes + You follow and comply with all Safe Quality Food (SQF) and Good Manufacturing Practices ( GMP 's). + You maintain mastery on ... + You perform responsibilities with and to maintain schedules, quality , and work place safety. + You perform other...an automated machinery environment + work in a USDA, FDA , OSHA, or GMP compliant environment **ESSENTIAL… more
    Conagra (08/15/25)
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  • Director, Inspection/Packaging

    Novo Nordisk (Bloomington, IN)
    …functions + Reviews and approves GMP documentation while ensuring safety and GMP quality compliance + Supports and leads continuous improvement projects + ... life-changing careers, and the opportunity to help improve the quality of life for millions of people around the...with company SOP's, specifications, as well as cGMP, ICH, FDA , EMA regulations or guidelines + Able to combine… more
    Novo Nordisk (07/25/25)
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  • Reliability Engineer

    ADM (Frankfort, IN)
    …flexible hours to support continuous production. (off hours, weekends, etc.) + Familiarity with GMP , FDA , and OSHA regulations is preferred + Must have knowledge ... to increase operational efficiency + Support and comply with all food safety, quality , and legality requirements + May perform reasonably similar or related duties… more
    ADM (07/23/25)
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  • Utilities Engineering Technician

    Lilly (Lebanon, IN)
    …facility, and the culture to enable a successful startup into GMP manufacturing operations. **Position Brand Description:** The Engineering Technician is responsible ... collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing site through start up. **Responsibilities:** Build and promote a strong… more
    Lilly (05/27/25)
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  • Forklift Operator - Receiving - Bakery Plant 3rd…

    Conagra (Indianapolis, IN)
    …to support quality work processes + Follow and comply with all Safe Quality Food (SQF) and Good Manufacturing Practices ( GMP 's). + Pick up and remove ... processing or packaging environment + Experience work in a USDA, FDA , OSHA, or GMP compliant environment **ESSENTIAL PHYSICAL AND MENTAL REQUIREMENTS:** + Sit,… more
    Conagra (07/16/25)
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  • Assembler II Farrar

    Trane Technologies (Noblesville, IN)
    …as needed. Ensure that device history records (DHR) are completed according to FDA GMP requirements. + Complete nonconformance records according to established ... + Promotes values as demonstrated in personal productivity and quality of work, management of internal/external relationships, actively seeking...procedures and GMP requirements. + Sheet Metal Assembly (using various assembly… more
    Trane Technologies (06/26/25)
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  • Technical Project Manager

    Bristol Myers Squibb (Indianapolis, IN)
    …projects ranging from $10 million to $150 million. * In-depth knowledge of GMP , FDA requirements, and regulatory considerations for radiopharmaceuticals. * Prior ... are delivered on schedule, within scope, and in compliance with regulatory and quality standards. This position reports directly to the Head of Program Management.… more
    Bristol Myers Squibb (08/12/25)
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  • Principal Engineer, Validation

    Novo Nordisk (Bloomington, IN)
    …to embark on life-changing careers, and the opportunity to help improve the quality of life for millions of people around the world. Our Bloomington, Indiana ... and/or Engineers + Strong understanding of guidance documents from FDA , EMA, PDA, ISPE, ASME, ISO, and other industry...+ 8+ years of Validation experience + 4 years GMP or regulated industry experience, required + Must be… more
    Novo Nordisk (08/13/25)
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  • Associate Scientist I, Microbiology

    Bristol Myers Squibb (Indianapolis, IN)
    …root causes and implement corrective actions as required. + Ensure compliance with GMP regulations, radiation safety guidelines, and quality standards. + Perform ... related field and 0-1 years of relevant experience in production or quality control in a cGMP/ FDA regulated facility. + A high school diploma may be acceptable… more
    Bristol Myers Squibb (07/26/25)
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