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The newly created Manufacturing Intelligence organization within Pfizer’s Global Technology & Engineering will help to drive Pfizer Global Supply toward ‘Industry 4.0’ capability through Big Data, Process Analytical Technology, Advanced Process Control, Artificial Intelligence and Robotics.
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The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century.
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This position will be responsible for metrology support for cGMP Clinical and Commercial Cell Therapy Manufacturing. This individual will partner with various Technical Operation functions in support of personalized cell therapy production through safe and compliant manufacturing operations according to cGMP requirements.
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Handle logistics and coordination of electrical construction activities as per engineering standards, vendor development, with the various departments like manufacturing, QA, QC, R&D for the engineering and Validation Aspects; maintain VMP and other GMP documents, Support Process Validation and Development Studies.
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Minimum of 5+ years of experience working with Pharmaceutical Manufacturing systems (e.g. Data solutions, MES technologies such as Rockwell Automation Pharma Suite, Emerson Syncade, Siemens Camstar, or Werum PAS-X.
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Firmly grounded in the rich heritage of Italian manufacturing excellence and an innovative perspective on the fusion of eyewear and fashion, they have transitioned from a humble "artisanal workshop" to establish themselves as prominent global leaders in the eyewear industry.
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Possess continuous improvement experience with emphasis in the laboratory information management and deployment of LEAN/Six Sigma, analytical methods and manufacturing process development for polymeric materials.
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Continuous innovation in passive component function integration, miniaturization, and manufacturing automation, cutting edge WSS and amplifier technology and comprehensive optical, mechanical, electrical and software integration capabilities enable us to serve the needs of high-density, high-bandwidth, and flexible optical networks.
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Reporting to the Global Quality Engineering Director, the Supplier Quality Specialist will achieve ALAM goals in the areas of manufacturing quality, technology advancement, productivity, off-spec elimination, non-conformance elimination, customer satisfaction, and cost reduction.
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This exciting new role works with the CAR-T Assets Maintenance & Calibration Manager and will be tasked with improving the Reliability and Maintainability of the assets supporting manufacturing operations onsite.
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The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconductor manufacturing, and metrology, to a broad range of scientific R&D and QC measurements.
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Reporting directly to the Senior Manager of Quality, this position collaborates closely with External Manufacturing Organizations (EMO), spanning pharmaceuticals, medical devices/combination products, consumer products/OTC, and biologics sectors, ensuring adherence to cGMP regulations and Bausch Health requirements.
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Specifically at the Branchburg site, this position would aid the site adoption and continued enhancement of new and existing systems including Manufacturing Execution Systems (MES), progressing the site's paperless manufacturing objective and Digital Plant Strategy.
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This position requires a solid technical understanding of drug substance process development and manufacturing, drug product formulation development and manufacturing, analytical methods development and validation, technology transfer and scale-up, process characterization and validation, clinical and commercial supply operations, and CMC regulatory and GMP compliance requirements.
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GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
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manufacturing job Title: packer Company: Jabil Circuit in Bridgewater, NJ
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