• 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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  • Senior Manager, Global Product Quality

    Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
    …a controlled way that is in accordance with regulatory expectations and applicable GMP /GDP quality standards. This role will provide specialized Biologics ... bioprocessing, purification, and formulation activities. + Responsible for the day-to-day quality oversight of assigned GMP contract manufacturers. + Responsible… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Associate Director, Global Product Quality

    Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
    …well as drive continuous improvement. **Job Description** + Responsible for directing quality oversight of GMP contract manufacturers of controlled substances ... **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP...batch record review and release process for + OAPI GMP release of Contract Manufacturers operations supporting clinical and… more
    Otsuka America Pharmaceutical Inc. (12/19/25)
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  • Sr. Specialist, External Manufacturing…

    Bristol Myers Squibb (Indianapolis, IN)
    Quality experience will be considered **Skills and Qualifications** + Expertise in GMP , Quality , material and product disposition + Strong capability in ... global leader in radiopharmaceuticals. **Summary** The Senior Specialist, External Manufacturing Quality Assurance is responsible for quality oversight of the… more
    Bristol Myers Squibb (11/20/25)
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