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We specialize in aluminum extrusion and fabrication, and we’re committed to delivering high-quality products through continuous improvement and advanced manufacturing techniques. Automation and Robotics: Develop and implement automation and robotics solutions to enhance manufacturing processes in aluminum extrusion and fabrication.
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The ideal candidate for this position should have work experience in cell therapy process development, manufacturing science, analytical development, and familiarity with GMP/FDA/ICH guidelines.
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Actively looking for a Senior Scientist, Cell Therapy Process Development contributing to the development of early and late stage clinical cell therapy manufacturing processes. Experience with common equipment used in cell therapy manufacturing such as Sepax, Lovo, G-Rex, Xuri Bioreactors, CliniMACs Plus, CliniMACS Prodigy, MaxCyte GT.
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The cell therapy process development team at is actively looking for a Senior Scientist, Cell Therapy Process Development contributing to the development of early and late stage clinical cell therapy manufacturing processes.
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Execute cGMP manufacturing activities, including CIP/SIP, media prep, cell culture sampling, and harvest operations. We are seeking a Consultant II with 3-5 years of experience in cell culture manufacturing within the biopharmaceutical industry.
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This role is pivotal in leading the design and execution of the Global Manufacturing & Supply (GMS) data governance process, from material creation to consumption across Warehouse, Materials Planning, Work Centers, Bill of Materials / Recipes, Costing and Quality Inspection attributes.
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Perform QC sampling and chemistry testing of raw materials under FDA/EU regulations, applicable International Regulations, processes and procedures to support GMP manufacturing. Perform QC sampling and chemistry laboratory testing of raw materials (starting materials, excipients, primary packaging, manufacturing water) to ensure timely generation and reporting of test results in support of manufacturing operations.
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Work experience in cell therapy process development, manufacturing science, analytical development, and familiarity with GMP/FDA/ICH guidelines. Develop and optimize cell therapy manufacturing processes from scratch or using existing processes.
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Experience in or as a driver, delivery driver, non CDL driver, general labor, landscaping, transportation, construction, production, manufacturing, factory, assembly or warehouse helpful. Experience in or as a driver, delivery driver, non CDL driver, general labor, landscaping, transportation, construction, production, manufacturing, factory, assembly or warehouse helpful.
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A background of pharmaceutical manufacturing or quality control/quality assurance is a plus. The candidate must possess Chemistry, Manufacturing and Controls (CMC) and CTD experience. He/she/they defines and manages the compilation of the documentation, required for the authoring by reaching out to appropriate internal/external functions such as quality, manufacturing, Global Regulatory Affairs (GRA), technical experts from global locations or contract manufacturing organizations (CMOs), or alliance partners.
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Associate Director, Tech Ops (Process Chemistry) will have responsibility for the management of API/Intermediate/RSM manufacturing operations at Insmed’s CMOs including tech transfer, process optimization, clinical/commercial manufacturing, process characterization and validation, and manufacturing CMC development strategy.
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Lead and drive the development of viral vector-based (e.g., AAV, lentivirus, retrovirus) manufacturing processes to improve efficiency, scalability, and product quality, with a focus on innovation and optimization.
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Experience in Food or Nutritional Food, Nutraceuticals, Dietary Supplements processing or manufacturing. manufacturing quality technician. Experience processing or manufacturing nutritional food formulations.
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Technical Writer II (Manufacturing/Quality) He/she/they defines and manages the compilation of the documentation, required for the authoring by reaching out to appropriate internal/external functions such as quality, manufacturing, Global Regulatory Affairs (GRA), technical experts from global.
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The validation scope comprises a multi-site global manufacturing network responsible for manufacturing an approved cell therapy product in the Multiple Myeloma space. Extensive experience in an approved cell therapy program with end-to-end know-how in support of validation in a global manufacturing network.
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pfizer manufacturing jobs in Belle Mead, NJ
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