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The successful candidate will oversee technical installation of Manufacturing Operational Technology (OT) hardware and software solutions that support Pharma Services Group (PSG) GxP compliant systems, including the following examples of OT devices Manufacturing Execution Systems, Computerized Maintenance Monitoring Systems, Advanced Analytic Systems, Serialization Systems, etc.
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A minimum of five (5) years 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, own the process knowledge of the cell and gene therapy manufacturing process technology to support technical activities for transfers into and out of the Raritan facility.
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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.
$20 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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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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All three major manufacturing departments utilize filtration technologies. Responsible for providing support to their respective process team, per Manufacturing Standard for Operational Excellence (MSOE) 602.
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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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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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Work with our software team on integration solutions for the manufacturing process and data management, including eBR, MES, QMS, and LIMS. We are seeking an innovative and highly motivated Senior Process Engineer on our MSAT team who will contribute significantly to the development of our advanced cell therapy manufacturing platform.
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Working conditions require the ability to sit, stand, walk, bend, climb stairs, and work at a computer station and on the manufacturing shop floor. Monitor, review, and improve manufacturing and quality-related activities and drive corrective and preventative actions.
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Experience in utilizing state of the art ERP systems and modern manufacturing technology experience, including RFID, barcoding, automated manufacturing equipment, etc. Evaluate operations processes, including order entry, manufacturing, time to close, PO process, and sales to revenue bookings processes to identify opportunities for automation, standardization, and improved cycle times.
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Experience with optical system design for manufacturing, design and cost. Act as an Optical Engineer for complex photonics programs in areas that can include free-space optical communications, laser transmitters for remote sensing, and RF photonics.
$180,000 - $220,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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The Manufacturing Supervisor role offers a dynamic opportunity to lead and train a team of operating personnel in the production of clinical or commercial products. Working knowledge of safety, quality systems, and cGMP Manufacturing packaging and or required.
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Our state-of-the-art facility complies with current Good Manufacturing Practice (cGMP) standards, ensuring our products' highest quality and safety. Your daily responsibilities will include: Execute Process Unit Operations: Follow standard operating procedures and batch records to perform essential manufacturing tasks.
$49,088 - $66,413 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Position Description: The Automation Engineer is primarily responsible for leading projects, the development and/or configuration of PLC/HMI codes, S88 batch recipe, historian data, historian reports, data analytics for reliable operation of manufacturing processes, and the existing automation systems, support for Building Management System (BMS), Utility and manufacturing process automation support for the Lilly New Jersey Facilities, as applicable.
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Global Pharmaceutical company, with US HQ in Central New Jersey, focused in Metabolics, Endocrinology and Oncology is expandingLooking for a strong Quality Assurance Manager for the entire North American manufacturing and quality organization.
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manufacturing job Title: manufacturing assistant Company: Ashley Furniture Industries Inc in Branchburg, NJ
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