• FSP - Research Scientist - Small Molecule…

    ThermoFisher Scientific (San Diego, CA)
    …such as degradation products and shelf-life extension. + Strong knowledge of specifications, method validation and transfer. + Previous stability management and ... on - now and in the future. Within our Analytical Services team, we have a functional service provider...project team or a working group. + Assists in method development and validation activities as needed.… more
    ThermoFisher Scientific (09/26/25)
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  • Associate Scientist , Analytical

    Guidehouse (Bethesda, MD)
    …and operating procedures of general laboratory equipment. + Experience with analytical equipment automation or instrument and method qualification will ... oral and written communication skills. + Proficiency in writing and reviewing method qualification/ validation protocols and reports, method transfers, SOPs,… more
    Guidehouse (10/04/25)
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  • Associate Scientist

    Catalent Pharma Solutions (Winchester, KY)
    … research and development work in the Analytical R&D Department. The Associate Scientist work/assist on method development, method transfer, method ... **Associate Scientist ** **Position Summary** Catalent, Inc. is a leading...client's documents as required including but not limited to specification/ validation reports/test methods/compliance reports etc. to perform gap analysis… more
    Catalent Pharma Solutions (09/25/25)
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  • Sr. Associate Scientist - Plate Based

    Actalent (Sanford, NC)
    …BasedJob Description The Sr. Associate Scientist will support the Quality Control Method Transfer and Validation team by performing method validation ... analytical needs and controls. + Engage with the method development team and participate in in-process and final...sections of technical reports to support interdepartmental technology and method validation and transfer processes. + Prepare… more
    Actalent (10/07/25)
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  • Quality Control Scientist - Microbiology,…

    Catalent Pharma Solutions (Princeton, NJ)
    …management, deviation/CAPA investigations, Change Controls, technology transfer, method validation /qualification, equipment maintenance, and cross-functional ... and commercial-scale autologous and allogeneic cell therapy production. The QC Scientist - Microbiology, Bio- Analytical and Raw Material is responsible… more
    Catalent Pharma Solutions (10/04/25)
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  • Associate Principal Scientist , Combination…

    Merck (Rahway, NJ)
    …others. + Proven track record of applying analytical skills in product test method design, development, and validation . + Working knowledge of analytical ... output(s) meet design input(s). + Lead establishment of test methodologies, including method development and validation , internally or externally, per design… more
    Merck (10/09/25)
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  • QC Scientist (pharma/micro)

    Astrix Technology (Wilmington, OH)
    …+ Support regulatory audits. + Write protocols and execute method verification/ validation /qualification/ transfers + Write, execute laboratory investigations ... **QC Scientist (pharma/micro)** Quality Control Wilmington, OH, US Pay...technical knowledge of microbiological / Chemistry test instrumentation and method development / validation including software/computer system… more
    Astrix Technology (10/12/25)
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  • Senior Scientist I

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …conducts reviews of routine and non-routine analyses of raw materials, by appropriate analytical methods. The Senior Scientist I works on complex technical ... studies, product investigations, troubleshooting of equipment, and other general research in analytical chemistry. The Senior Scientist I serves as a technical… more
    The US Pharmacopeial Convention (USP) (09/09/25)
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  • mRNA Quality Control Scientist

    Sanofi Group (Waltham, MA)
    …US site and externally at Contract Testing Laboratories (CTL) for various QC and analytical activities. The QC Scientist will support with both GMP and GLP ... **Job Title:** Quality Control Scientist **Location:** Waltham, MA **About the Job** At...of GMP and non-GMP batches + Support Raw material method development, qualification, and/or validation of methods… more
    Sanofi Group (10/15/25)
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  • Chromatography Principal Scientist

    Sanofi Group (Cambridge, MA)
    …Extensive experience in method development using HPLC/UPLC and GC + Experience in analytical method validation + Record of adhering to and promoting lab ... is seeking a highly motivated individual to join our analytical group as a **Chromatography Principal Scientist **...technical reports independently + Share knowledge and experience of analytical method development for synthetic molecules +… more
    Sanofi Group (10/10/25)
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