• Scientist IV, Cheminformatics

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …engineering knowledge, statistical analysis, and data-driven decision-making into pharmaceutical supply chain management, synthesis optimization, and PAT solutions ... advanced supply chain solutions. Use of normalization, mean-centering, and cross- validation strategies to ensure model robustness and interpretability while managing… more
    The US Pharmacopeial Convention (USP) (08/13/25)
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  • Associate Director, Viral Vector Downstream…

    Gilead Sciences, Inc. (Oceanside, CA)
    …against metrics + Partner with Vector Process Development, Quality, Validation , Engineering, Maintenance, BSO, MSAT, and Supply Chain (Warehouse/Materials ... and 2+ years of experience in manufacturing in the pharmaceutical industry OR + A MS/MA and 8+ years...with senior leaders + Strong knowledge of quality systems, validation principles, regulatory guidelines, and multi-product controls + Experience… more
    Gilead Sciences, Inc. (07/31/25)
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  • Manufacturing Associate II, Upstream Processing

    Endo International (Horsham, PA)
    …is responsible for supporting necessary fermentation and production activities, including validation and development work as needed. All incumbents are responsible ... procedures are followed. + Assists with process, equipment, and cleaning validation initiatives. + Assists in leading manufacturing activity as needed. Documentation… more
    Endo International (09/20/25)
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  • Scientist - Bioanalytical

    Actalent (Sanford, NC)
    …Description The Scientist will support the Quality Control Method Transfer and Validation team by performing method validation activities, including drafting ... sections of technical reports to support interdepartmental technology and method validation and transfer processes. + Prepare technical reports, critically review… more
    Actalent (09/19/25)
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  • Senior Scientist, Biomarker Laboratory, Mass…

    BeOne Medicines (San Carlos, CA)
    …join our Clinical Biomarker laboratory. This role will lead the development, validation , and execution of quantitative and qualitative mass spectrometry assays to ... well as hands-on experience in mass spectrometry-based biomarker method development, validation and clinical sample analysis. **Essential Functions of the job:** +… more
    BeOne Medicines (09/16/25)
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  • Jt817 - Quality Applications Spec

    Quality Consulting Group (Villalba, PR)
    QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... industry in Puerto Rico & USA. Responsibilities: + Conducts a compliant validation process for quality information technology systems which requires formal … more
    Quality Consulting Group (09/13/25)
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  • MES Test Engineer, Project Kuiper

    Amazon (Bellevue, WA)
    …for Manufacturing Execution System (MES) applications, ensuring robust validation of functionality, performance, and integration before production deployment. ... across MES applications Perform load/stress testing using NeoLoad for performance validation Design and maintain automated test scripts for regression testing Create… more
    Amazon (09/13/25)
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  • Manufacturing Associate I, Manufacturing Support…

    Endo International (Horsham, PA)
    …responsible for supporting necessary production and production-related activities, including validation and development work as needed. All incumbents are ... and computer applications. + Assists with process, equipment, and cleaning validation protocols. Investigation + Assists in the resolution of manufacturing… more
    Endo International (09/10/25)
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  • CQV Specialist - Upstream Process Equipment…

    Mentor Technical Group (Juncos, PR)
    …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... America. Key Responsibilities: + Develop, review, and execute qualification and validation protocols (IQ, OQ, PQ) for upstream and downstream process equipment.… more
    Mentor Technical Group (09/07/25)
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  • Quality Engineer II - Design & Reliability…

    Integra LifeSciences (Braintree, MA)
    …documentation such as product requirements, schematics, verification, and validation strategy/execution. + Coordinate and review development documentation created ... SPC programs with Manufacturing and Quality Control as a part of Process Validation and Design Transfer. + Knowledgeable of and applies statistical analysis to… more
    Integra LifeSciences (09/06/25)
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