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Conduct process development, optimization and scale-up studies; bring this knowledge to project teams to enable successful drug product technology transfer to clinical manufacturing and commercial sites.
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The scientist will also ensure the transfer of robust manufacturing processes to CMO from Bristol Myers Squibb (BMS) Product Development (PD)/ Global Product Development and Supply (GPS) or CMO. The scientist will also ensure robust process performance at CMO during commercial manufacture by use of continuous process verification, Operational Excellence (OPEX) principles, etc.
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Driving the beverage cart to different areas on the golf course to service food and beverage to guest. The Beverage Cart Driver is integral to the guest experience and provides food and beverage services (both alcoholic and non.
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Knowledge of design for manufacturing and part fabrication techniques, including CNC machining (milling/turning), EDM, injection molding, and rapid prototyping. Experience with hands-on machining & fabrication, including milling, turning, additive manufacturing, and assembly.
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Handling day-to-day activities inclusive of project execution and management, vendor management, data management, life cycle management, issues, deviations, corrections, remediation and improvement efforts within the plant of all computerized systems such as SAP, MES, manufacturing and laboratory equipment, BAS, EDS and other software, systems and associated interfaces.
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We are actively seeking a proficient SAP Master Data Governance Lead with a specific focus on Materials orchestration throughout the End-to-End Manufacturing & Supply lifecycle. 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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Participate in design and implementation of manufacturing processes from the laboratory and concept stage through pilot plant and manufacturing scale-up. We serve all global regions and every step of device manufacturing within each segment of the electronics supply chain.
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CGMP manufacturing experience, preferably cell/gene therapy, with experience in tech transfer, process validation, project management, and change management. This individual will oversee process engineering, manufacturing support, technology transfer, validation, and cell therapy automation and provide technical and continuous improvement support to ensure robust production, testing, and the timely release of cost-effective, compliant, and high-quality cell therapy products.
$170,000 - $220,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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The ideal candidate for this position will have extensive experience in process engineering, SPC, MSA, GD&T, DOE, metal stamping, laser welding, metal forming, injection molding, CNC, scrap reduction, process engineering management, continuous improvement, budgeting/forecasting, training, mechanical design, manufacturing, writing test procedures, and GR&R.
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This position would be responsible for providing support services to the WIC certification process and food delivery of food benefits to eligible participants assisting in Nutrition Education.
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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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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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Develop expertise on key continuity themes in Manufacturing, Supply Chain, Facilities and across Development and manage the inter-dependencies with Quality, IT (Cyber security), Third Party Risk Mgmt.
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Intermediate knowledge of pharmaceutical manufacturing and utilities that support cell therapy clinical manufacturing. Thorough knowledge and hands-on experience in commissioning and qualification of manufacturing facilities: REQUIRED – manufacturing rooms, material path-throughs; Thorough knowledge and hands-on experience in commissioning and qualification of common utilities: compressed air, carbon dioxide, process air, AHUs; PREFERRED – liquid nitrogen supply systems, DI Water.
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The Injection Molding Process Engineer is a "hands-on" position that plans, directs, and coordinates manufacturing equipment and processes to produce high-quality injection molded products. Strong and diverse technical background in injection molding processing, tooling, equipment, materials, manufacturing, and quality.
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