• Senior Scientist

    Lundbeck (Bothell, WA)
    …acid analyzer. Share responsibility for equipment maintenance and upkeep. + Review DNA sequencing data (including NGS), Southern/Northern blots, quantitative ... PCR results. + Author and review cell line development technical reports that meet expectations...ability to effectively and independently manage laboratory work and data , including capturing data accurately in appropriate… more
    Lundbeck (08/27/25)
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  • Sci III - Upstream Process Development

    ThermoFisher Scientific (Plainville, MA)
    …on multiple programs with minimal direction. Lead project timelines and tasks. + Technically review data , collaborate with customers on data and experimental ... documentation skills, proven track record to analyze and interpret data to draw conclusions and make recommendations, and strong...quality by design (QbD) and regulatory needs in the pharmaceutical industry, + A flexible work schedule may be… more
    ThermoFisher Scientific (08/17/25)
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  • Director, Early Clinical Leader - Cardiovascular…

    Bayer (Cambridge, MA)
    …focused clinical development plans and studies to produce timely and high-quality data ; + Proven achievement and innovation in pharmaceutical medicine, with ... indication and medical need, as well as medical/clinical interpretation of study data and additional relevant information; + Lead expert panel meetings and advisory… more
    Bayer (08/15/25)
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  • Senior Associate Scientist - Principal…

    Charles River Laboratories (Ashland, OH)
    …to minimize study impact, with minimal oversight. * Prepare summary of method development data , with minimal oversight. * Execute review and approval of data ... complexity, to include study management, interpretation, and reporting of study data , and assuring the regulatory compliance of these projects. ESSENTIAL DUTIES… more
    Charles River Laboratories (07/30/25)
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  • Lead Technician-QC-IDM

    Lilly (Indianapolis, IN)
    …associated with laboratory operations and batch release qualification and associated workshops. + Review IDM QC Lab data using ALCOA+ principles, as well as ... Prior experience with scheduling and training. + Prior experience with batch and/or data GMP review /release Education Requirements: High School diploma or GED… more
    Lilly (09/16/25)
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  • Director, Global Regulatory Labeling Strategy

    Takeda Pharmaceuticals (Boston, MA)
    …executes a labeling implementation plan to incorporate new scientific, safety and clinical data , as well as Health Authority responses / feedback into CCDS, USPI and ... Responsible for working with direct reports to develop and/or review the labeling implementation plan ensuring that the most...(MSc, PhD, or PharmD) preferred. + 10+ years of pharmaceutical industry experience. This is inclusive of 8 years… more
    Takeda Pharmaceuticals (09/10/25)
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  • Principal Scientist 2 - ARD

    Cambrex High Point (High Point, NC)
    …final product that are validatable . Maintain laboratory notebook and perform data review . Maintain lab instrumentation. Conduct method development and ... methods for intermediates and final product. + Maintain and review notebook and data entries. + Write...Working knowledge of other analytical equipment common to the pharmaceutical industry This position works with and handles hazardous… more
    Cambrex High Point (09/04/25)
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  • Quality Control Associate I, Bioanalytical…

    Charles River Laboratories (Cleveland, OH)
    …Chemistry Team at our Safety Assessment site located in Cleveland, OH. Perform QC review of study data and perform inspections. Monitor and track common errors ... but are not limited to, those listed:_ + Efficiently review all procedures, materials, and results in compliance with...as well as perform QC reviews of daily study data in one QC discipline. + Perform lab walk… more
    Charles River Laboratories (09/03/25)
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  • Clinical Research Quality Specialist B (Department…

    University of Pennsylvania (Philadelphia, PA)
    …members to facilitate and conduct high quality compliance reviews, which include review preparation, conduct, close out and reporting, to ensure compliance with ... This position will interface with research investigators and staff throughout the review process. Within the OCR, the Clinical Research Quality Specialist will… more
    University of Pennsylvania (08/03/25)
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  • QA Lead Technical Operations - CAPA

    Sokol Materials & Services (Skillman, NJ)
    …communication skills are required. + Background in problem solving + Knowledge of Data integrity principles + Proven attention to details + Comfortable working in an ... using a solid understanding of Quality Systems and regulatory requirements. * Review and approve documents related to Quality, Quality Control, Validation, and… more
    Sokol Materials & Services (07/31/25)
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