• Daiichi Sankyo, Inc. (Bernards, NJ)
    …for direct reports, and mentors DM Operations Data Validation and Reporting staff.Directs programming representation in audits and regulatory inspections ... and immune disorders. Job Summary: The Director of Data Management (DM) Reporting provides leadership in Data Management Operations for the Data Validation and… more
    HireLifeScience (10/27/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Category Sourcing Lead as part of the Global Operations team based in Raritan, NJ. Role ... innovation, pioneering work and evolving best practices.The Global Sourcing Category Lead is responsible for leading global sourcing activities for direct materials… more
    HireLifeScience (10/30/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …in Raritan, NJ. Role OverviewThis position will be responsible for providing project lead support for strategic initiatives and capacity expansion activities ... and priorities of the plant. This position will also be responsible for establishing and reporting on key project /program metrics in support of on time and on… more
    HireLifeScience (08/09/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …CAPA Management Process for the respective business areas.Responsibilities:Leadership and Project Management: Lead the end-to-end quality execution across Medical ... centered around rare diseases and immune disorders. Job Summary: Reporting to the Sr. Director, Medical Affairs QA, the...leading global projects with high impact with ability to lead and project -manage cross-functionally and globally with… more
    HireLifeScience (09/03/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …timelines.Develop quality systems and procedures for the signaling activities to assure regulatory compliance and meet regulatory reporting timelines. ... regulatory authorities. Provides compliance metrics to management, as needed. Lead continuous improvement around development of new signal workflow/process,… more
    HireLifeScience (09/03/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …Raritan, NJ. Role OverviewThe Associate MES Engineer will be part of MSAT team reporting to the Manufacturing Execution Systems Lead and will be responsible for ... Global Procedures.Support Site Readiness of MES for FDA and/or Other Regulatory Audits / Inspections.Establish key stakeholder relationships with internal and… more
    HireLifeScience (08/28/25)
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  • Genscript USA Inc. (Piscataway, NJ)
    …site staff, contractors, and project teams. Support permit applications and regulatory reporting . Lead site inspections, audits, and emergency drills. ... federal regulations. The ideal candidate will have strong experience in construction project support, including providing EHS input during early design and planning… more
    HireLifeScience (09/15/25)
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  • Merck & Co. (Rahway, NJ)
    …ONSITE 3 DAYS PER WEEK)The Submissions Content Source Management Business Operations Lead is expected to understand the end-to-end regulatory submission process. ... lead and influence others outside of a direct reporting relationshipBroad organizational awareness and knowledge of touch points/interdependenciesDemonstrated… more
    HireLifeScience (11/01/25)
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  • Merck & Co. (Rahway, NJ)
    …supervision of management.- Lead a team of staff assigned to the project as needed.-This includes the following activities:1. Is involved in late clinical ... reports to effectively communicate results of clinical trials to the project team, Management, regulatory agencies, or individual investigators.9. Provides… more
    HireLifeScience (10/27/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …systems and track training completion rates to ensure compliance with safety and regulatory requirements Lead the development and delivery of training on case ... processing, safety reporting , and relevant regulatory guidelines (FDA, EMA,...make adjustments based on feedback, compliance audits, and evolving regulatory standards Key Area #2 Lead the… more
    HireLifeScience (10/28/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From healthcare provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
    HireLifeScience (10/28/25)
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  • Merck & Co. (Rahway, NJ)
    …and 3rd party logistics sites, supply chain and technology teams, and regulatory and project leaders. The successful candidate will demonstrate ownership ... Job DescriptionDirector, Packaging Shipping Systems (Logistics and Distribution Technology) Reporting into the Director Packaging Distribution, Components and Systems… more
    HireLifeScience (10/16/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From healthcare provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
    HireLifeScience (10/28/25)
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  • Regulatory Reporting Lead

    Motion Recruitment Partners (New York, NY)
    Regulatory Reporting Lead / Project Manager New York, NY **Hybrid** Contract $90/hr - $96/hr Grow your career with an innovative global bank in New York, ... NY as an Regulatory Reporting Project Manager. Contract role with strong possibility of extension. Will require working onsite 2-3 days per week. Join one of… more
    Motion Recruitment Partners (10/10/25)
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  • Manager - Financial Services Risk Management…

    Deloitte (New York, NY)
    Manager, Regulatory Reporting Our Deloitte Regulatory , Risk & Forensic team helps client leaders translate multifaceted risk and an evolving regulatory ... 2025 Work You'll Do As a Manager, you will lead teams and client engagements across Deloitte's global network,...directing projects related to the implementation and automation of regulatory reporting processes, ensuring rigorous testing and… more
    Deloitte (11/01/25)
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  • Senior Consultant - Financial Services Risk…

    Deloitte (Morristown, NJ)
    Senior Consultant, Regulatory Reporting Our Deloitte Regulatory , Risk & Forensic team helps client leaders translate multifaceted risk and an evolving ... and validating reporting data, developing quality assurance programs, and remediating regulatory reporting issues + Defining regulatory reporting more
    Deloitte (09/05/25)
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  • Manager- Financial Regulatory

    American Express (New York, NY)
    …Financial Reporting Quality Assurance Organization (FRQA), in support of the Regulatory Reporting Automation program. This role is responsible for driving ... quick thinkers who can shape the strategic decisions that lead our business forward. Whether it's negotiating with some...leading program and change governance efforts for finance / regulatory reporting platforms. This role will support… more
    American Express (10/31/25)
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  • Strategic Initiative Lead

    Sanofi Group (Morristown, NJ)
    **Job Title:** Strategic Initiative Lead - Regulatory Data, Digital and AI **Location** : Cambridge, MA or Morristown, NJ **About the Job** Do you thrive at the ... opportunities, transforming concepts into business-ready solutions that future-proof Sanofi's Global Regulatory Affairs (GRA). Reporting to the Head of… more
    Sanofi Group (10/16/25)
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  • Broker Dealer Regulatory Governance…

    SMBC (New York, NY)
    …support across the Advisory Function with respect to broker-dealer-applicable regulatory engagements, support function coordination, governance and reporting . ... Change Management + Compliance Alerts and other Communications Governance and Reporting : The Regulatory Governance Team is responsible for producing management… more
    SMBC (10/09/25)
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  • Global IVD Regulatory Center of Excellence…

    Pfizer (New York, NY)
    reporting and decision-making. Your expertise will help resolve project issues, guide operational teams, and facilitate agreements across the enterprise. ... resource requirements (people, financial, technology) for projects across the IVD Regulatory COE/Portfolio. + Lead and support cross-functional issue resolution… more
    Pfizer (11/02/25)
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