- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Batch Warehouse Associate Manager as part of the Quality team based in Raritan, NJ. ... of incoming Apheresis, Raw material, Spot check, pack out of final product material.Develop positive relationships with the QA team, Quality Control, Information… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …The Position We are seeking a dynamic and experienced Regulatory Affairs Labeling Associate Manager to oversee and lead critical tasks related to final ... education and collecting data to support efficacy and new product development, CMR is involved. The one thing that...requires labeling verification to include the review across the product family of physician and patient leaflets, carton and… more
- Merck & Co. (Rahway, NJ)
- …operational/executional arms within the business. The Program Clinical Supplies Project Manager serves as the primary program-level Global Clinical Supply point of ... development related meetings.- Working independently, the Program Clinical Supplies Project Manager designs strategic and operational plans for all clinical supply… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director, Global Business Process Manager , Global DX is responsible ... processes, continuous optimization, and digitalization, in collaboration with the Transformation Manager for process automation.- Define and deliver a global BPM… more
- Genmab (Plainsboro, NJ)
- …essential to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager / Associate Director will be responsible for leading the development ... Safety Information (CSI), United States Package Inserts (USPI), Summary of Product Characteristics (SmPC), and their associated Patient Labeling Documents.Serve as… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The one thing that keeps us all marching to ... a living. Are you ready to make a difference? The Position The Associate Director, Regulatory Affairs - Advertising & Promotion will provide strategic regulatory… more
- Aequor (Thousand Oaks, CA)
- …of full product manufacturing stages experience. The Supply Chain Project Manager (SCPM) will translate product variation strategy as determined by the ... Lead for reportable changes for Global Distribution control. May also translate product launch/variation strategy as determined by the Regional Operations Lead to an… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Associate Director, CMO Operation as part of the Global Manufacturing and Supply ... vein team (V2V) to plan, schedule and track the manufacture of autologous cell product batches at CMOMonitor the progress of product batches, identify and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …team on all aspects of statistical activities; collaborates closely with data manager to ensure high quality data.- Drug Development Strategy: Provides input to ... scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile.- CRO / Vendor Oversight: Review CRO/vendor proposal and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …around rare diseases and immune disorders.Summary Under the guidance of the ( Associate ) Director, the Manager , US Medical Affairs Oncology will contribute ... to development of the US medical affairs plan for assigned product (s) and ensure optimal execution of planned activities. This includes strategic partnerships with… more
