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Deploys Lean Manufacturing techniques in the area of quality, cost reduction, complete and on-time deliveries, safety, customer satisfaction, employee relations, visual controls and plant performance measures.
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A background of pharmaceutical manufacturing or quality control/quality assurance is a plus. He/she/they defines and manages the compilation of the documentation, required for the authoring by reaching out to appropriate internal/external functions such as quality, manufacturing, Global Regulatory Affairs (GRA), technical experts from global locations or contract manufacturing organizations (CMOs), or alliance partners.
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Support Quality Systems such as; change control, deviation, CAPA, audits, quality metrics, etc. This role will be a hands-on resource reporting to the Quality Control Manager.
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The Quality Assurance Document Control Specialist role is an exempt position responsible for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.
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Knowledge of quality systems (GxP, ISO, Lean, TPS, etc.) Then consider joining us as a Quality and Safety Manager in Piscataway, New Jersey! 1+ years of Continuous Improvement experience using Lean Six Sigma and 5S methodologies.
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Substantial knowledge of Quality Systems, GMP, FDA, GAMP, ISO and other applicable standards. Experience with Operational Excellence and/or Lean Manufacturing. cGMP manufacturing experience, preferably cell/gene therapy, with experience in tech transfer, process validation, project management, and change management.
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This role is pivotal in leading the design and execution 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 CNC Machinist Programmer will be responsible for operating several CNC machining tools to produce a variety of precision parts to support our growing sales of industrial drying equipment and systems.
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Intermediate experience with Operational Excellence and Lean Manufacturing. Collaborates with SMEs from the Development Group, Global MSAT Group, Supply Chain Group, Manufacturing Group, and Quality Group while providing technical support for the resolution of process deviations, the evaluation and implementation of process changes and continuous improvement support to the production operations to ensure rapid, flawless, compliant, and cost-effective delivery of quality products.
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Associates or no degree required with 4 or more years of experience working in the pharmaceutical industry in Quality Control/Assurance or Manufacturing, and 2 or more years in a leadership role.
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Maintenance & Facilities Manager oversees and coordinates the day-to-day maintenance and repair of buildings, grounds, utilities services to the building and equipment within manufacturing, packaging, and distribution sites to ensure that all facility/utility systems are operating safely and within code.
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5+ years' experience in Supply Chain, Operations, Project Management, or Portfolio Management in Finance, Manufacturing, or Quality Operations environments. Keywords : project portfolio manager, PPM, PPM lead, project portfolio lead, finance, financial lead, finance SME, finance subject matter expert, excel, macros, performance tracking, financial tracking, supply chain quality, global PMO, project management, PM, analytical, strategic, business manager, analytics, OGSM, sharepoint, planisware, tableau, QSMR, performance improvement, P&L, profit and loss, risk mitigation, opex, CIP, capex.
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The Helium System includes the Amarillo, TX wellfields & crude helium reservoir (Bush Dome), the crude helium production plant, and the 400+ mile Crude Helium Pipeline that runs form Amarillo, TX to Bushton, KS with third-party owned plants connected along the way that inject crude helium into the pipeline and/or remove crude helium from the pipeline.
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Demonstrated hands-on product development experience and knowledge in Dairy & Dairy Alternative Category Application segment (Yogurt & Fermented Milk products, Cheese, Ice Cream, Frozen Desserts, Ready-to-Drink Beverages, and their Plant-Based Alternatives)Knowledge of ingredient selection and differentiation related to selecting and formulating with Starches, Hydrocolloids, Proteins, Specialty Sweeteners, Flavors, Enzymes, and Cultures regarding Dairy and Dairy Alternative applications.
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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.
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plant lean manufacturing quality systems jobs Title: manager Company: Shamrock Foods Company in Bridgewater, NJ
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