• Associate Director, Global Labeling

    Takeda Pharmaceuticals (Trenton, NJ)
    …order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director, Global Labeling Lead where you will be responsible for the ... Labeling Lead , coordinates the process to obtain labeling approval by Labeling Senior Management Cross-functional team ( Global Labeling more
    Takeda Pharmaceuticals (01/15/25)
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  • Global Labeling Lead

    Merck (Rahway, NJ)
    …the prevention and treatment of diseases in people and animals. In the capacity of a Global Labeling Lead , you will be instrumental in shaping the ... to demonstrate your superior execution skills. **Core Responsibilities** + As a Global Labeling Lead , you will guide cross-functional teams in the creation,… more
    Merck (01/15/25)
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  • Director, Global Labeling Strategy…

    Takeda Pharmaceuticals (Trenton, NJ)
    …plasma-derived therapies for patients with immunologic, hematologic, and other complex diseases. The Director, Global Labeling Strategy Lead is a key role in ... the process to obtain labeling approval by Labeling Senior Management Cross-functional team ( Global... Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk… more
    Takeda Pharmaceuticals (01/26/25)
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  • Senior Manager, Global

    Takeda Pharmaceuticals (Trenton, NJ)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as the Senior Manager, Global Labeling Devices. You will be responsible for ... Labeling Lead , coordinates the process to obtain IFU labeling approval by Labeling Senior Management Cross-functional team ( Global Labeling more
    Takeda Pharmaceuticals (01/17/25)
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  • Sr . Director, PV Medical Surveillance

    Taiho Oncology (Princeton, NJ)
    Sr . Director, PV Medical Surveillance Princeton, NJ, USA Req #378 Monday, July 15, 2024 Looking for a chance to make a meaningful difference in the oncology space? ... we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other....on a transformative journey with Taiho Oncology as a Sr . Director, PV Medical Surveillance . At the forefront… more
    Taiho Oncology (01/13/25)
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  • Senior Director, CAR-T Global

    J&J Family of Companies (Raritan, NJ)
    …responsible for commercial leadership on the compound development team (CDT) and global labeling teams. The Commercial Leader, CAR-T, contributes to optimizing ... Johnson & Johnson is recruiting for a Senior Director, CAR-T Global Marketing and...Lymphoma, Leukemia and Cell Therapy Commercial Strategy and will lead a cross-functional, highly matrixed global commercial… more
    J&J Family of Companies (01/28/25)
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  • Senior Director, Oncology R&D

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders. **Summary** The Senior Director sits within Global Oncology Clinical Development, an ... **Clinical Development Expertise Strategy:** + In collaboration with the Global Clinical Lead (GCL), if applicable, leads...Health Authority) + Participant and voting member in the labeling development process in the Labeling Working… more
    Daiichi Sankyo Inc. (01/01/25)
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  • Senior Buyer/Planner, Production Planning

    Endo International (Cranbury, NJ)
    …R&D, IT and Commercial and the Manufacturing Operations ERP business systems lead . Senior Buyer/Planner is responsible for material planning, purchasing, and ... develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering… more
    Endo International (01/10/25)
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  • Senior Manager, Regulatory Affairs…

    Gilead Sciences, Inc. (Parsippany, NJ)
    …Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across ... agencies. You will represent RA Ad/Promo in Regulatory Project Teams and labeling meetings; providing strategic regulatory guidance and seeking advice as needed from… more
    Gilead Sciences, Inc. (01/28/25)
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  • Executive Director, Global Clinical Supply,…

    Merck (Rahway, NJ)
    **Job Description** The Global Clinical Supply (GCS) organization, within our Research & Development (R&D) Division, is accountable for managing the 'end-to-end' ... and External Collaborations (~200+). GCS is accountable for the planning, sourcing, labeling , packaging and delivery of clinical supplies to clinical sites across… more
    Merck (01/24/25)
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  • Senior AV Field Engineer:

    Diversified (Kenilworth, NJ)
    Senior AV Field Engineer: Kenilworth, NJ Kenilworth, NJ, USA Req #3970 Wednesday, January 22, 2025 At Diversified, we don't just follow tech trends - we set them by ... companies around the globe Founded in 1993, we're a global organization serving local needs with associates worldwide. Learn...What part will you play? Under general direction, the Senior Field Engineer will oversee commissioning of large and… more
    Diversified (01/24/25)
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  • Medical Director, Global Medical Safety…

    Takeda Pharmaceuticals (Trenton, NJ)
    …my knowledge. **Job Description** **Objective:** **Principal responsibilities include:** + Serves as Global Safety Lead (GSL) and the Company-wide patient safety ... well as other labeling documents. + Demonstrate knowledge of local and global health authority requirements. + Support GPSE in the maintenance of a highly… more
    Takeda Pharmaceuticals (01/24/25)
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  • Executive Director, Global Clinical Supply,…

    Merck (Rahway, NJ)
    **Job Description** The Global Clinical Supply (GCS) organization, within our Research & Development (R&D) Division, is accountable for managing the 'end-to-end' ... and External Collaborations (~200+). GCS is accountable for the planning, sourcing, labeling , packaging and delivery of clinical supplies to clinical sites across… more
    Merck (01/24/25)
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  • Compliance Specialist

    Carter's/OshKosh (New York, NY)
    …career at Carter's. **HOW YOU'LL MAKE AN IMPACT:** This role typically reports into the Sr Director, Quality Assurance and is based in our Skip Hop New York office. ... into the office 3 days a week. 40%: Regulatory Labeling , Warnings, and Restrictions + Act as subject matter...and annual stuffed article licenses per state. + Manage global registrations, sampling and payments to keep registrations current.… more
    Carter's/OshKosh (01/17/25)
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  • Associate Director, Clinical Supply Project…

    Merck (Rahway, NJ)
    …internal and external to Global Clinical Supply and serves as the lead Global Clinical Supply spokesperson at clinical and development related meetings. ... not limited to:** + Interacts closely with key partner organizations (as a lead Global Clinical Supply Planning program representative) such as clinical… more
    Merck (01/16/25)
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  • Director, Regulatory Affairs

    Sumitomo Pharma (Trenton, NJ)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... Regulatory Affairs** . The Director is part of the Global Regulatory Affairs (GRA) team based in the US....(GRL) for assigned projects. This position is expected to lead the development and implementation of regulatory strategy from… more
    Sumitomo Pharma (11/28/24)
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  • Assistant General Counsel, Market Access

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …of Company and/or departmental expectations and goals as identified by senior management. **Responsibilities** - Lead drafting and negotiating contracts ... people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...external outside counsel. - Serve as a member of Labeling and Pricing Committees and as legal representative on… more
    Daiichi Sankyo Inc. (11/16/24)
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  • Director - Patient Centered Outcomes Research…

    Novo Nordisk (Plainsboro, NJ)
    …US organization. Relationships The Director-Patient Centered Outcomes Research reports directly to a Senior Director within the CDSE RWE team. This is a US affiliate ... (MAPA), as well as collaborating where appropriate with therapeutically aligned global counterparts in Medical Science, Patient Focused Drug Development, Data… more
    Novo Nordisk (01/22/25)
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