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The Sr. Director, Quality Technical Operations, Cell Therapy Manufacturing is responsible for leading the day-to-day quality review and approval of investigations, CAPA, Change Controls with associated documents and the oversight of the Quality Engineering team responsible for qualifications and validations of computerized systems, software, enterprise systems, equipment, methods, and manufacturing processes.
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Are you an EHS Manager looking to take the next step in your career and become a Regional EHS Manager within a Food Manufacturing company? If so, please read on and apply to the EHS Manager - Food Manufacturing - Bilingual job based in Newark, NJ.
$120,000 - $140,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We specialize in electrical discharge machining (EDM) and precision manufacturing of all mechanical components for the aerospace and medical device industries as well as tooling for the plastics industry and stamping industry.
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Job DescriptionJob DescriptionWHO WE ARE:We are a textile recycling/manufacturing company located in Irvington, NJ specializing in Food Packaging for Shipping of Refrigerated and Frozen ingredients as well as the manufacturing of Mattress Components and Insulator Pads by recycling fibers.
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Provides GMP engineering services in a pharmaceutical manufacturing setting. Bachelors Degree in Engineering or related field 3-4 years experience in Pharmaceutical/ Manufacturing setting Basic use of tools/ equipment.
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Experience in an industrial setting such as petrochemical or power plant, commercial construction, concrete, sandblasting, hydro-blasting, coating application, painting, or manufacturing environment preferred.
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Microsoft Dynamics 365 Manufacturing Manager. Crowe's Consulting Manufacturing and Distribution practice has an exciting opportunity for a D365 Finance & SCM T&L Manager to join our growing team.
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Senior Project Manager Cell Therapy Development and Operations / Manufacturing. As a certified PMP with a breadth of hands-on project management experience in the Pharma/Biotech/Cell Therapy regulated environments, the CTDO Sr. PM is expected to perform with minimal supervision and effectively facilitate the successful delivery of a wide process development and commercialization activities within the CTDO organization from initiation to completion while remaining aligned with company strategy, commitments and goals.
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Understanding of GMP and FDA regulatory requirements correlating to biologics. 5+ years of experience in CAR T / Cell Therapy or Biologics. Cell Therapy Development and Operations Senior Project Manager (CTDO Sr. PM) will influence and manage all aspects of initiating, planning, and executing complex, multi-disciplinary CTDO projects throughout the projects lifecycle.
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Provides Engineering Support required for supporting Mechanical, Electrical & Plumbing (MEP) manufacturing related utility systems inclusive of HVAC, Steam, Chilled Water, Compressed/Process/Breathing Air, Liquid Nitrogen, CO2, Electrical (Normal, UPS, Emergency Generator), etc.
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Drive project management and portfolio solutions across cell therapy technical operations team. Familiarity/experience with end-to-end CMC drug development. Experience with sharepoint, Smart Sheets, ServiceNow, etc.
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As a certified PMP with a breadth of hands-on project management experience in the Pharma/Biotech/Cell Therapy regulated environments, the CTDO Senior PM is expected to perform with minimal supervision and effectively facilitate the successful delivery of a wide process development and commercialization activities within the CTDO organization from initiation to completion while remaining aligned with company strategy, commitments and goals.
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We are seeking an experienced power press set up technician to join our Linden, NJ based manufacturing facility. The ideal candidate will have experience in manufacturing, tool and die shop environment.
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Our highly respected precision metal stamping company is seeking a Program Manager with at least 5 years’ experience in a manufacturing and/or product design (R&D) environment. Knowledge of TQM, Six Sigma or Lean Manufacturing principles preferable.
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Experience in biologics process development and process characterization to enable efficient tech transfer to manufacturing sites. The candidate should have experience with technology transfer to facilitate scale-up of early phase and late phase biologic drug product manufacturing processes to GMP production facilities.
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manufacturing job Title: engineer Company: Marriott in Summit, NJ
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