• Vice President, Quantitative Credit Risk Modeler

    SMBC (Jersey City, NJ)
    …risk models for wholesale and commercial portfolios, ensuring alignment with regulatory requirements (eg, CCAR/DFAST, CECL, Basel III/IV) and business objectives. ... possess strong technical expertise in quantitative modeling, a deep understanding of regulatory frameworks, and the ability to collaborate across risk, finance, and… more
    SMBC (08/13/25)
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  • Scientific Director, Global Diagnostic Lead,…

    J&J Family of Companies (Raritan, NJ)
    …all assets within Heme, ensuring alignment with overall clinical development and regulatory activities. + Serve as the primary point of accountability for diagnostic ... including ensuring in-stream data quality from partners. + Work with colleagues in Regulatory Affairs to ensure that all relevant regulatory documents (eg IDEs,… more
    J&J Family of Companies (08/13/25)
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  • Associate Director, Device Technology

    Merck (Rahway, NJ)
    …in alignment with the company's business goals, and quality and regulatory compliance. **Essential Duties and Responsibilities:** + Utilize extensive experience in ... in both development and lifecycle management, ensuring compliance with relevant regulatory standards. + Ensure robust technical plans, risk communication, drive… more
    Merck (08/08/25)
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  • Director, Combination Product Commercialization

    Merck (Rahway, NJ)
    …in alignment with the company's business goals, and quality and regulatory compliance. **Essential Duties and Responsibilities:** _Strategic Leadership and Project ... collaboratively with receiving sites, drug product partners, and Technical Product Leaders, regulatory and quality. + Provide Voice of Manufacturing input to early… more
    Merck (08/08/25)
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  • Associate Director, GVP Audits

    Gilead Sciences, Inc. (Parsippany, NJ)
    …regarding audit outcomes and CAPAs. Beyond auditing, this role supports regulatory inspections, readiness, and partners with the R&D Quality Extended Leadership ... improvements in R&D quality processes, systems, and standards to meet regulatory requirements and organizational goals while contributing to the overall quality… more
    Gilead Sciences, Inc. (08/08/25)
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  • Principal/Sr Principal Scientist, Hematology Lead…

    Bristol Myers Squibb (Princeton, NJ)
    …translational data generated to support asset development and contribute to regulatory submissions. This individual will work on cross-functional project teams to ... and disease scientists and BMS members from clinical, medical, commercial, regulatory and diagnostics as well as engage external academic collaborators/Key opinion… more
    Bristol Myers Squibb (08/08/25)
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  • Principal Sterilization Microbiologist

    System One (Park Ridge, NJ)
    …direction, leading high-impact sterilization programs, and ensuring full regulatory compliance across the product lifecycle-from development through ... testing when necessary. Your expertise will directly impact product safety, regulatory success, and speed-to-market for critical medical devices and healthcare… more
    System One (06/26/25)
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  • Senior Scientist/Principal Scientist, Oncology…

    Bristol Myers Squibb (Princeton, NJ)
    …space + Manages relationships with key internal stakeholders including Regulatory , Clinical, Commercial, Medical Affairs & Communications and external collaborators ... in high quality scientific, technical or medical journals **Qualifications** : + PhD degree in a relevant field (eg molecular biology, cancer biology, human… more
    Bristol Myers Squibb (08/17/25)
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  • Senior Principal Scientist/Associate Director,…

    Bristol Myers Squibb (Princeton, NJ)
    …oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external ... in high quality scientific, technical or medical journals. **Qualifications** : + PhD degree in a relevant field (eg molecular biology, cancer biology, human… more
    Bristol Myers Squibb (08/14/25)
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  • Associate Director, Neuroscience, Clinical…

    Bristol Myers Squibb (Princeton, NJ)
    …activities for the pipeline and supports late stage portfolio for regulatory , translational development and life cycle management. Translational Development drives ... Participates in post-hoc biomarker analysis and publication efforts + Supports regulatory submissions and regulatory interactions as needed **Skills/Knowledge… more
    Bristol Myers Squibb (08/22/25)
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