• Enterprise Test Automation Product Manager

    Lilly (Indianapolis, IN)
    …play a crucial role in ensuring the quality and reliability of our pharmaceutical software products across the enterprise. You will lead automation testing efforts, ... and JMeter. + Familiar with database testing and SQL scripting for data validation . + Understanding of authentication and identity protocols such as OAuth and OpenID… more
    Lilly (07/29/25)
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  • Data Review Assistant I

    Charles River Laboratories (Reno, NV)
    …Coordinates all laboratory support, pre-study activities, method development, method validation , study activities, data and/or reporting activities. Responsible for ... our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic… more
    Charles River Laboratories (07/29/25)
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  • Scientist III - Regulated Immunogenicity…

    Parexel (PA)
    …on method development reports and test method optimization, qualification and validation . + Strong organizational and project management skills. + Demonstrates ... Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals… more
    Parexel (07/26/25)
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  • Laboratory Equipment IT Engineer, Regeneron Cell…

    Regeneron Pharmaceuticals (Cambridge, MA)
    …with automation systems and control system software + Support engineering and validation projects as well as provide support to manufacturing activities with process ... in a manufacturing/lab/IT setting. Must have experience in a pharmaceutical or biopharmaceutical manufacturing facility. Must have experience with automated… more
    Regeneron Pharmaceuticals (07/26/25)
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  • Senior Manufacturing Systems BRM

    Abbott (Columbus, OH)
    …+ 10 years of IT experience in large or midsized multinational Pharmaceutical , or Health Care organization software development and manufacturing systems + ... projects ranging from $1MM-$5MM. + Experience with **IQ/OQ/PQ** , validation documentation, and execution and GxP environments Apply Now… more
    Abbott (07/26/25)
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  • Senior Director, Precision Medicine Search,…

    Bristol Myers Squibb (Princeton, NJ)
    …degree, eg, MSc, PhD. Specific experience in the diagnostic and pharmaceutical industries, oncology biomarkers, and diagnostic business development. Minimum of 10+ ... years' experience in assay and IVD development including analytical validation , clinical development, manufacturing, US and global regulatory submission, and… more
    Bristol Myers Squibb (07/24/25)
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  • Staff Manufacturing Engineer - Shockwave

    J&J Family of Companies (Santa Clara, CA)
    …for existing products. + Support the transfer of product lines and the qualification- validation efforts. + Other duties as assigned. These job requirements are not ... in a medical device environment or equivalent experience in other industries ( pharmaceutical or automotive) that use the same principles of operation and similar… more
    J&J Family of Companies (07/23/25)
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  • Maintenance Manager, Integrated Powder

    Reckitt (Zeeland, MI)
    …+ Knowledgeable in regulatory requirements and equipment system qualification and validation . + Significant experience in powder and liquid processing and packaging ... of food products, preferably within a highly regulated food or pharmaceutical environment. Promote a culture that prioritizes food safety in all organizational… more
    Reckitt (07/23/25)
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  • CLIA Laboratory Director (Board Certified…

    GRAIL (Durham, NC)
    …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... for new test development + Review and approves the technical performance validation and verification reports for new tests, instruments, and methods prior to… more
    GRAIL (07/22/25)
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  • Director II, Clinical Development

    AbbVie (Irvine, CA)
    …regulatory submissions and responses and other program documents. Lead development, validation , and justification of new clinical outcome assessment instruments for ... supervision. + At least 5 years of clinical study experience in the pharmaceutical industry, academia, or equivalent. + Ability to oversee a complex clinical… more
    AbbVie (07/22/25)
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