• Associate Director of Validation

    Bristol Myers Squibb (Indianapolis, IN)
    …(>$10M). + Demonstrated understanding and hands-on experience with radiopharmaceutical or pharmaceutical validation systems and compliance. + Direct experience ... and external contractors. **Skills and Qualifications** + Strong knowledge of pharmaceutical validation practices, including cGMP and FDA/USP/OSHA regulatory… more
    Bristol Myers Squibb (11/26/25)
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  • Director, Commercial Manufacturing…

    Sumitomo Pharma (Indianapolis, IN)
    … of the following activities - equipment and utilities qualification/ validation , process development, process validation , continued process ... 8 - 12 years (with Master's) of relevant experience in biotech or pharmaceutical industry Validation experience with multiple therapeutic modalities (eg API,… more
    Sumitomo Pharma (12/12/25)
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  • Machine Learning Scientist/Sr Scientist, Federated…

    Lilly (Indianapolis, IN)
    …access to machine learning models trained on Lilly's extensive proprietary pharmaceutical research data. Through federated learning, the platform enables Lilly to ... biotech partners. The Machine Learning Scientist/Sr Scientist, Federated Benchmarking & Validation Engineering plays an essential role within the TuneLab platform,… more
    Lilly (10/30/25)
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  • Sr Manager - Validation Lead - Technical…

    Lilly (Indianapolis, IN)
    …of progressive experience in business analytics, data science, product delivery, or validation -related roles within the pharmaceutical or technology industry. + ... methodologies. + Experience with IT Solution Delivery and Support, Computer Systems Validation , and process optimization. + Strong communication, leadership, and… more
    Lilly (01/17/26)
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  • Scientist I - Method Validation

    Bristol Myers Squibb (Indianapolis, IN)
    …field + Minimum 5 years of experience in analytical method development, validation , verification, and transfer in the pharmaceutical or radiopharmaceutical ... a Bristol Myers Squibb company, is looking for a Scientist I - Method Validation at their Indianapolis manufacturing site. The person will be responsible for method… more
    Bristol Myers Squibb (01/08/26)
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  • Validation Engineer II

    PACIV (Indianapolis, IN)
    …Writing, or Information Systems) + Minimum 8 years proven experience in validation documentation within regulated environments (eg, pharmaceutical , biotech, or ... Validation Engineer II PACIV stands for P rocess...V alidation. As a global leader in industrial automation, process control solutions and instrumentation, we serve clients in… more
    PACIV (01/06/26)
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  • DeltaV Tech Lead - ( Pharmaceutical

    Cognizant (Indianapolis, IN)
    …in cross-functional program leadership meetings, ensuring alignment between automation, process engineering, digital/MES, and quality teams + Serve as the ... software testing strategies + Identification of any remediation effort required on process control software + Identify and analyze risks of technical nature… more
    Cognizant (01/06/26)
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  • Senior Principal Engineer - Automation Engineering…

    Lilly (Lebanon, IN)
    …control team, including design, controls philosophy, implementation and commissioning * Process control validation testing, implementation and coordination * ... provide CSV support leading and executing CSV activities for process automation systems across the site. This role will...Develop and implement the Automation Engineering Project Validation Plan. * Provide subject matter expertise for computer… more
    Lilly (12/13/25)
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  • Business Process Architect (BPA) MQ IT, GSC

    Lilly (Indianapolis, IN)
    …making of medicine "with safety first and quality always". As the Business Process Architect, you will be a strategic technology leader responsible for aligning ... end-users and addressing their needs promptly. + Maintain computer system validation for responsible applications. + Deliver recommendations to implement improved… more
    Lilly (01/07/26)
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  • Scientist - API Manufacturing Process

    Lilly (Indianapolis, IN)
    … variability and capability. + Understand, justify and document the state of validation ( process and cleaning) with data that evaluate the capability of ... to achieve the reliable and compliant manufacture of the Active Pharmaceutical Ingredient External Manufacturing (API EM) portfolio which includes raw materials,… more
    Lilly (01/09/26)
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