• Novo Nordisk Inc. (West Lebanon, IN)
    …entering our sterile cleanroom areas while following all relevant gowning, safety, and quality policies. Prior experience in a GMP environment or life science ... department in cross-functional teams (Manufacturing, Engineering, Technical Support and Quality groups) and present relevant material during audits/inspections Participate… more
    HireLifeScience (10/30/25)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …The Logistic Associate will provide multi-faceted support to materials, quality , procurement, warehouse, and manufacturing operations. Daily routine will consist ... be expected to have strong documentation skills and a quality focused mindset, in order to prepare for potential...for potential internal or external audits in line with GMP and FDA requirements. Incumbent will be expected to… more
    HireLifeScience (11/26/25)
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  • Novo Nordisk Inc. (West Lebanon, IN)
    …to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. The Manufacturing Technician will be expected ... cleanroom areas, and follow all relevant gowning, safety, and quality policies. When technicians are not working in cleanroom...covers, snood, face mask, sterile gloves, and to follow GMP processes at all times. Examples of prohibited materials… more
    HireLifeScience (11/08/25)
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  • Director, Global Quality GMP

    Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
    The Director, Global Product Quality , GMP Processes is a strategic leadership role responsible for **benchmarking, standardizing, and optimizing global ... quality systems are aligned with **Good Manufacturing Practices ( GMP )** and regulatory requirements while driving **efficiency, consistency, and continuous… more
    Otsuka America Pharmaceutical Inc. (12/16/25)
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  • Principal Specialist, Quality Assurance

    Cardinal Health (Indianapolis, IN)
    quality and compliance. + Provides ideas for continuous improvement of the GMP Quality Management System. + Escalates complex issues to management in a ... for raw material, work in process, and finished products. + Champion Quality , GMP compliance and EHS/Radiation Safety practices. + Develop and lead GMP more
    Cardinal Health (11/25/25)
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  • Quality Assurance Supervisor

    Meijer (Middlebury, IN)
    …to assure facility compliance to corporate, regulatory and best in class industry quality , GMP (Good Manufacturing Practices), SQF (Safe Quality Foods), ... job profile below and apply today! Plans, organizes, executes, and monitors quality assurance activities for assigned facility. Assists in the development and… more
    Meijer (12/04/25)
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  • Quality Line Inspector

    Cardinal Health (Indianapolis, IN)
    …evaluate their potential impact on product quality and compliance + Champion Quality , GMP compliance and EHS/Radiation Safety practices + Ability to network ... **_What Quality Assurance contributes to Cardinal Health_** Quality...Performs real-time QA review of batch documentation and other GMP related documents. + Issuance and reconciliation of product… more
    Cardinal Health (10/22/25)
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  • Engineer - Fume & CSQ Prd Quality Assurance

    Lilly (Indianapolis, IN)
    …deliverables. + Influence and oversee GMP drawings including review and approval of GMP drawings + Evaluate potential product quality impact for any GMP ... nature and assure issues are addressed appropriately. + Perform Quality approvals of GMP documents such as Critical Alarm Audits, Utilities Reports, Business… more
    Lilly (12/04/25)
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  • Senior Director Quality Control

    Lilly (Lebanon, IN)
    …to influence and implement the technical agenda, site business plan objectives, and GMP Quality Plan objectives + Interact with regulators, customers, or other ... to build the processes and facility to enable a successful startup into GMP manufacturing operations._ **Main Purpose and Objectives:** The Senior Director - … more
    Lilly (12/16/25)
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  • Associate Director, Global Product Quality

    Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
    …as well as drive continuous improvement. **Job Description** + Responsible for directing quality oversight of GMP contract manufacturers of Otsuka clinical and ... **Job Summary** The Associate Director, Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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