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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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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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The newly created Manufacturing Intelligence organization within company’s Global Technology & Engineering will help to drive company Global Supply toward ‘Industry 4.0’ capability through Big Data, Process Analytical Technology, Advanced Process Control, Artificial Intelligence and Robotics.
$25 - $32 an hourFull-timeExpandApply NowActive JobUpdated 4 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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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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Responsible for ensuring a stable supply of global/local products by managing the day-to-day relationship with Contract Manufacturing Organizations (CMOs) and Global supply chain members.
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Prior experience in a GMP quality (Manufacturing/QA/QC) environment, experience in drug substance, drug product and final packaged product a plus. Bausch Health is a global company that develops, manufactures, and markets a differentiated product portfolio across multiple high-growth therapeutic areas including Gastroenterology, Generics, Neurology, Ortho Dermatologics, Medical Aesthetics and Dentistry.
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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 Bedminster, NJ
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