• Representative, Quality Assurance- 11am-7:30pm Mon…

    Novo Nordisk (Bloomington, IN)
    …on the floor + Perform audits of manufacturing and support areas, including in-process batch record review for adherence to internal procedures and Good ... logbooks and resolving issues that occur during manufacturing + Review batch documents + Review ... Review /Disposition (DP and DS) + Reviews executed batch records + Dispositions product with delegation… more
    Novo Nordisk (08/08/25)
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  • Associate Representative, Quality Assurance- 4/3…

    Novo Nordisk (Bloomington, IN)
    …+ Assist with revision of GMP documentation such as Standard Operating Procedures, Master Batch Record review and SMPs + Initiate deviations as required ... Perform audits of manufacturing and support areas, including in-process batch record review for adherence...and approval of project related documents such as Master Batch Production Records , technical transfer, and process… more
    Novo Nordisk (08/08/25)
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  • Specialist II, Formulation / Filling Tues.-Fri., 6…

    Novo Nordisk (Bloomington, IN)
    …to solve issues presented in BRs during Analyst review + Assists QA Batch Record Review with Client Observations, including priority observations from QA ... of all types of GMP Documentation including Master Batch Records , Engineering Studies, Logbooks, Forms, etc....specific area for the purpose of material readiness, and record review + Assists supply chain in… more
    Novo Nordisk (07/23/25)
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  • Specialist I, Form/Fill (Weekend PM Shift for SL3)

    Novo Nordisk (Bloomington, IN)
    …IT related issues, and offers suggestions for new/improved equipment + Assists QA Batch Record Review with Client Observations, including priority ... issues and suggest solutions + Authors and/or approves Standard Operating Procedures (SOPs), Batch Production Records (BPRs) and reports + Ability to lead… more
    Novo Nordisk (06/12/25)
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  • Principal Representative, QA-Microbiology

    Novo Nordisk (Bloomington, IN)
    …group has oversight of the manufacturing areas, including process technology transfer, master batch record review and approval, on-the-floor support, product ... management, site-wide systems training, internal and external auditing, project review for accuracy and compliance, and material disposition. Quality Assurance… more
    Novo Nordisk (07/25/25)
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  • Packaging Technician

    Adecco US, Inc. (Indianapolis, IN)
    …products independently and approve in-process products at other stations. * Review batch paperwork and follow supervisor instructions to understand ... The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security… more
    Adecco US, Inc. (08/08/25)
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  • Packaging Technician

    Adecco US, Inc. (Indianapolis, IN)
    …products independently and approve in-process products at other stations. * Review batch paperwork and follow supervisor instructions to understand ... The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security… more
    Adecco US, Inc. (08/01/25)
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  • Sr. Manufacturing Operations Associate

    Lilly (Lebanon, IN)
    …stakeholders. + Support authoring and revision of standard operating procedures and batch records as required. Review technical reports. Conduct ... chillers, cooling towers, compressed air, distillation, tank transfer operation, batch processes, truck/rail operations) + Demonstrated operational capability with… more
    Lilly (08/08/25)
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  • Associate Director, MSAT, Upstream

    Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
    …+ Provide expert technical oversight of upstream manufacturing operations at CDMOs, including review of batch records , deviation investigations, and change ... of upstream process changes and improvements post-approval. + Author and/or review technical reports, protocols, risk assessments, and relevant sections of… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Associate Director, MSAT, Downstream Drug…

    Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
    …+ Provide expert technical oversight of downstream manufacturing operations at CDMOs, including review of batch records , deviation investigations, and change ... of downstream process changes and improvements post-approval. + Author and/or review technical reports, protocols, risk assessments, and relevant sections of… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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