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This role is pivotal in leading the design 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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We serve all global regions and every step of device manufacturing within each segment of the electronics supply chain. As a global supplier to the semiconductor industry, we provide advanced copper interconnects, die attachment, wafer bump processes, solder technologies, fluxes, cleaners, and other attachment materials for the integrated circuit fabrication, semiconductor packaging, and electronic assembly industries.
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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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The newly created Manufacturing Intelligence organization within Client's Global Technology & Engineering will help to drive Client Global Supply toward 'Industry 4.0' capability through Big Data, Process Analytical Technology, Advanced Process Control, Artificial Intelligence and Robotics.
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Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.
$170,000 - $220,000 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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A trusted partner of world leaders in the retail, manufacturing, distribution, travel, services and software industries, Sonata’s software portfolio includes the Brick & Click Retail Platform©, Modern Distribution Platform©, Rezopia Digital Travel Platform©, Kartopia E-commerce Platform©, Halosys enterprise development automation Platform©, CTRM Commodity Trading and Risk Management Platform© and KODO - AI Powered Customer Experience (CX) Platform.
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Specialist, QA Operations, is responsible for quality oversight of Cell Therapy Development Operations (CTDO) activities in accordance with BMS policies, standards, procedures, and Global cGMP requirements.
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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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Global Supply toward ‘Industry 4.0’ capability through Big Data, Process Analytical Technology, Advanced Process Control, Artificial Intelligence and Robotics. Good knowledge of pharmaceutical manufacturing and related unit operations is also a plus.
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In this site-facing lead role, you will partner with the Global Lilly Unified Lab (LUNA) program to deliver milestones across multiple workstreams such as Product Delivery, Master Data Management, Integration to Site Manufacturing and Quality Systems, Instrument Connectivity, and Organizational Change Management.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Specialist, QA Operations, is responsible for quality oversight of Cell Therapy Development Operations (CTDO) activities in accordance with Client policies, standards, procedures, and Global cGMP requirements.
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A minimum of 5 years of operations or quality Assurance experience within a cGMP environment in the biotech/biopharma industry and Cell/Gene Therapy cGMP manufacturing experience preferred. Provide technical expertise in the Technical Operations group, process knowledge of the cell and gene therapy manufacturing, including but not limited to deviations (Quality Issues), investigations, CAPA management.
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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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Proclinical Staffing is seeking a QC Investigation Specialist (Level 1, 2, 3, & Senior) to join a global biotech company. The QC Investigations Specialist, CAR-T Manufacturing is an exempt level position with responsibilities for leading deviations and corrective actions in support of the QC testing laboratories related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment.
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Actively contribute to the development of regulatory strategies for investigational products in Investigational New Drug (IND)/ Clinical Trial Applications (CTA), Biologics Licensing Application (BLAs)/ Marketing Authorization Application (MAA), through evaluating scientific merits of Chemistry, Manufacturing and Control (CMC) and nonclinical study data package.
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manufacturing global jobs in Raritan, NJ
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