• Senior Process Engineer II - CEA Controls

    Integra LifeSciences (Princeton, NJ)
    …Collaboration:** + Collaborate closely with cross-functional teams (eg, quality assurance, regulatory affairs , R&D, production) to ensure contamination control ... Process Engineer II a focus on manufacturing contamination control in the medical device industry. The successful candidate will be responsible for partnering with… more
    Integra LifeSciences (04/04/25)
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  • Director, MSAT Validation & Digital

    J&J Family of Companies (Raritan, NJ)
    …Collaboration:** + Work closely with cross-functional teams, including Quality Assurance, Regulatory Affairs , and IT, to align validation activities with ... of advanced validation strategies and frameworks to ensure compliance with regulatory standards. + Identify opportunities for process automation and digital… more
    J&J Family of Companies (06/06/25)
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  • Digital Biomarker Operational Lead

    Sanofi Group (Morristown, NJ)
    …through interaction with vendors and departments involved (Clinical Dev, Regulatory Affairs , Patient Perspective, Competitive Intelligence, BD, alliance ... Leads, Project Leads, Global Study Managers, Procurement, Vendor excellence, quality, regulatory , and other relevant teams to ensure study success. The Digital… more
    Sanofi Group (06/04/25)
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  • Director, HCP Marketing - Orgovyx

    Sumitomo Pharma (Trenton, NJ)
    …and peer-to-peer education. + Collaborate cross-functionally with Sales, Sales Training, Medical Affairs , Market Access, Omnichannel, Patient Marketing, Legal, ... salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical , dental, vision, life and disability insurances and leaves provided in… more
    Sumitomo Pharma (05/01/25)
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  • Director, Product & Pipeline Communications

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …demonstrated track record of successful product launch experience in the pharmaceutical/ medical device other related healthcare industry, strong business and media ... products (branded/unbranded) as well as planning around key data announcements, regulatory milestones and launch programs for late-stage pipeline candidates +… more
    Otsuka America Pharmaceutical Inc. (04/24/25)
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  • Lead Intellectual Property Counsel

    Dr. Reddy's Laboratories (Princeton, NJ)
    …will require extensive interaction with Portfolio, R&D, Business Development, and Regulatory Affairs . **Responsibilities:** + Manage patent litigations in North ... medicines more affordable to discovering innovative treatment options to satisfy unmet medical needs, we are dedicated to helping people lead longer and healthier… more
    Dr. Reddy's Laboratories (06/10/25)
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  • Senior Fraud Investigator

    Guardian Life (Holmdel, NJ)
    …We drive a high-performance culture across our Legal, Compliance, and Government Affairs functions, aligned to "what" we deliver (ie, our goals and objectives) ... investigative reports, including findings, recommendations, corrective actions and required regulatory filings, including, but not limited to Suspicious Activity… more
    Guardian Life (06/06/25)
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  • Senior Scientist, Preclinical Development-…

    Merck (Rahway, NJ)
    …interfacing with other functional areas (eg project management, manufacturing, quality, regulatory affairs ) and external partners to drive project milestones ... experimental design & data analysis, authoring of technical reports, regulatory submissions and patent applications. Active participation on formulation development… more
    Merck (06/04/25)
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  • Remote Solutions Architect

    Insight Global (Titusville, NJ)
    …experience as a Solutions Architect - Pharmaceutical industry experience focusing on Regulatory Affairs Technology projects - Integration and design for ... person will be joining a large team responsible for Regulatory Technologies. This person will work across a few...start on the 31st day of employment and include medical , dental, and vision insurance, as well as HSA,… more
    Insight Global (06/04/25)
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  • Senior Director, Clinical Research,…

    Merck (Rahway, NJ)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director May… more
    Merck (05/24/25)
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