• Executive Director, Head of Pharmacovigilance…

    Bristol Myers Squibb (Princeton, NJ)
    …labeling strategies. + Act as the key PV representative for interactions with global regulatory authorities and stakeholders, advocating for patient safety. + ... benefit-risk assessment, and aggregate safety reporting. + Experience interacting with global regulatory authorities and scientific advisory bodies **Preferred… more
    Bristol Myers Squibb (07/08/25)
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  • VP Clinical Development, Oncology

    Sumitomo Pharma (Trenton, NJ)
    …Interface with regulatory authorities, including the FDA, EMA, and other global agencies, to secure trial approvals and navigate the regulatory landscape. ... strategy for Oncology, aligning with SMPA's overall goals and regulatory requirements. + Lead the medical and...data and present findings clearly. + Significant experience with global clinical trials and regulatory process. +… more
    Sumitomo Pharma (08/14/25)
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  • Director, Human Resources Executive Compensation

    Integra LifeSciences (Princeton, NJ)
    …relation to executive compensation alignment, retention strategies, and harmonizing HR policies. ** Global Equity and Incentive Programs:** + Lead the design and ... with local and global standards. + Stay informed about market trends, regulatory changes, and best practices to ensure that the company's Total Rewards offerings… more
    Integra LifeSciences (07/23/25)
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  • Scientific Director/Senior Scientific Director,…

    Bristol Myers Squibb (New Brunswick, NJ)
    …innovative solutions to complex CMC technical challenges. + Strong knowledge of global regulatory guidelines and requirements (eg, FDA, EMA, ICH guidelines). ... Project Team objectives and encompass drug substance, drug product, analytical, quality, regulatory , and clinical supplies. + Represents the Global Product… more
    Bristol Myers Squibb (08/22/25)
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  • Senior Director, Quality Risk Management…

    J&J Family of Companies (New Brunswick, NJ)
    …Quality Risk Management & External Engagement has oversight for the Regulatory Intelligence Programs in Clinical and Commercial Manufacturing (GxP, GMP, cGMP), ... design and implementation of an effective and proactive Risk Management & Regulatory Intelligence framework to optimally prepare and support the Innovative Medicine… more
    J&J Family of Companies (08/22/25)
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  • Associate Director, GVP Audits

    Gilead Sciences, Inc. (Parsippany, NJ)
    …or external reviews including ensuring alignment with Gilead business needs and regulatory requirements. + Stay current with evolving global PV regulations ... audits, supporting E-System/Digital audits, as well as, support or lead complex audits across the broader R&D, vendor, and...the biopharma or related industry. + Proficiency in pharmacovigilance regulatory requirements ( Global ) is a must. +… more
    Gilead Sciences, Inc. (08/08/25)
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  • Director, GCP Audits

    Gilead Sciences, Inc. (Parsippany, NJ)
    …10+ Years with MS/MA or MBA **PREFERRED QUALIFICATIONs:** + Proficiency in clinical regulatory requirements ( Global ) is a must. + Expert-level experience working ... audit activities and deliverables across large sites, countries, or multiple regions. + Lead internal and external R&D quality audits for assigned R&D groups or… more
    Gilead Sciences, Inc. (08/21/25)
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  • Compliance Risk Assessment Manager

    TD Bank (Mount Laurel, NJ)
    …industry standards. **Role Description:** + Supports the US Compliance Risk Assessment lead with managing and facilitating the US Compliance Risk Assessment and ... management of the Compliance Risk Assessment framework to ensure the applicable regulatory compliance risks and internal controls are identified and assessed to… more
    TD Bank (08/23/25)
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  • Director - Packaging Technology

    Sanofi Group (Morristown, NJ)
    …of Sanofi's Global Medical Device and Packaging organization is to lead the industry in device-mediated therapies, with the ambition to develop, launch and ... and deploy robust manufacturing solutions. May act as Manufacturing Lead on large scale global projects. +...validation plan and execution of IQ/OQ/PQ in accordance with regulatory , company & site requirements. Will often support sites… more
    Sanofi Group (08/08/25)
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  • Program Manager, AML Compliance

    Coinbase (Trenton, NJ)
    …to monitor the success of the compliance Program and track adherence to global regulatory requirements. * Utilize an in-depth understanding of metrics, ... This role involves leading strategic, multi-regional Programs to ensure compliance with global AML regulatory bodies. The Program Manager will ensure the… more
    Coinbase (08/09/25)
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