• 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 ... area management and quality management + Acts as QA reviewer on Minor deviations + Identify continuous improvement initiatives... Review /Disposition (DP and DS) + Reviews executed batch records + Dispositions product with delegation… more
    Novo Nordisk (08/08/25)
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  • Specialist II, Formulation / Filling WAM Fri-Sun 8…

    Novo Nordisk (Bloomington, IN)
    …IT related issues, and offers suggestions for new/improved equipment + Assist QA Batch Record Review with Client Observations, including priority ... Associate + Review and Approve new client batch records + Create, review ,...BRs during Analyst review + Assists QA Batch Record Review with Client… more
    Novo Nordisk (08/15/25)
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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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  • Lead, Inspection Sun-Fri 11 PM - 7:30 AM

    Novo Nordisk (Bloomington, IN)
    …to the Manager to be added as required + Review all activities within the Master Batch Record (MBR) throughout the shift, at the end of shift and at the end ... equipment in accordance with cGMPs + General understanding of batch records and following procedures based off...following procedures based off the steps provided in a batch record + Troubleshoot basic equipment and… more
    Novo Nordisk (07/18/25)
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  • Quality Documentation Specialist

    Dairy Farmers of America (Richmond, IN)
    …Description** **GENERAL PURPOSE** Review specifications, procedures, protocols, and batch records for Good Manufacturing Procedures (GMPs) compliance to ... regulatory review findings . File and maintain batch production and control records . Inform...and company computer systems . Able to keep good records ( record keeping skill) . Able to… more
    Dairy Farmers of America (08/01/25)
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  • Operator III, Inspection Sun-Fri 11 PM-7:30 AM

    Novo Nordisk (Bloomington, IN)
    …in EDMS + Review Label Control specific activities within the Master Batch Record (MBR) to ensure effective and accurate communication of production ... visual factory + Required to read, understand, follow, and review GMP documents + Leads area continuous improvement activities...+ Reviews all non-equipment specific activities within the Master Batch Record (MBR) throughout the shift to… more
    Novo Nordisk (07/18/25)
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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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  • QA Representative API EM

    Lilly (Indianapolis, IN)
    Review and approve documents such as procedures, production records , change control proposals, deviations, equipment qualifications, analytical methods, and ... Overview:** The QA - API provides support to all quality activities including batch disposition of API batches at Contract Manufacturing organizations (CMs). The QA… more
    Lilly (06/03/25)
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  • Sr. MES Opcenter OR Camstar Consultant - Remote

    Cognizant (Indianapolis, IN)
    …in the Medical Device and pharmaceutical manufacturing industries Understand the paper Batch record and business process flow in collaboration with business ... 5 and/or following the client Quality standards. Author and review test scripts (IQ, OQ, PQ) Perform IQ (application...designs into OpCenter by looking through existing documentation (paper Batch Records ) **Why Join Us:** + Opportunity… more
    Cognizant (07/18/25)
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