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Apply the Process Safety Management (PSM) regulations to day to day operations and capital project work. Demonstrated strong leadership skills, in project and people management in a continuous improvement environment in the areas of production, safety, quality and Lean manufacturing principles.
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Travel to suppliers, fabricators, or other locations to perform process inspections, conduct factory testing or review fabrication issues/improvement opportunities. Knowledge of ISO quality systems as well as improvement tools such as Lean Manufacturing and Six Sigma preferred.
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As the Senior Accountant, Abbott Nutrition Corporate Financial Services (CFS) Record to Report (RTR) you will be responsible to prepare journal entries, prepare monthly consolidated reporting packages and other analysis supporting the Nutrition division; serve as liaison between our Shared Service Third Party provider, FP&A and CFS RTR; and drive process improvements.
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Maintain knowledge of and visibility to the sales crediting process and business rules of the franchise, including: data sources, market definitions, alignments, filtering for on-label specialties [ABS], and the Best Address Process.
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If you are ever unsure about what is being required of you during the application process or its source, please contact HR Shared Services at 866-278-6942 or HRSharedServices@brunswick.com. Please let us know if you require accommodations during the interview process.
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Collaborate with Shift Leader and Continuous Improvement & Process Manager to brainstorm continuous improvement ideas to maximize productivity and efficiencies. Communicate planned and unplanned activities with the process manager and department production monitoring system (Barco.
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Process Mold Technician 1. Identify and document process parameters (such as hot runner controls). Set molds, startup and shut down injection molding machines, and understand basic injection molding machine functions as specified by work order or setup parameter sheet meeting all requirements such as correct sequence, proper setup, shutdown, mold storage, and lockout-tag out procedures.
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The ideal candidate will have an understanding of the PPAP process and experience in creating and editing PPAP documents, including Control Plans. Responsibilities include ensuring all quality documentation is submitted on time, potentially handling some corrective action reporting, and updating PPAP documentation and Control Plans throughout the engineering process.
$34 - $43.5 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Manage and process customer attestation requests, such as but not limited to: Certificate of Origin, Food Grade, Specification Sheet, Nutritional, Allergen, GMO/Non-GMO, CoO, CoA, SDS, Shelf-Life Ext, etc.
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In this role, you will act as the Sterility Assurance Project Lead, driving new product development, sustaining product support, and manufacturing facility margin improvement projects. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
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Supports the Fresenius Kidney Care (FKC) commitment to the Quality Indicators and Outcomes and Quality Assessment and Improvement (QAI) Activities, including those related to patient satisfaction and quality of life and actively participates in process improvement activities that enhance the likelihood that patients will achieve the FKC Quality Goals.
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Follow Client's Quality Manual, SOPs, and Environmental Health, Safety & Sustainability (EHS&S) guidelines in day-to-day activities, to ensure proactive compliance and continuous improvement. Follow Client's Quality Manual, SOPs, and Environmental Health, Safety & Sustainability (EHS&S) guidelines in day-to-day activities, to ensure proactive compliance and continuous improvement.
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We have built a solid record of successful long term strategic partnerships with our customers by bringing innovative and sustainable solutions to their businesses year over year with our process driven approach to create flawless operational delivery.
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The Human Factors (HF) group manages the drug delivery device user interface design process and executes usability assessments required to support the successful submission of Combination Products.
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Utilize Continuous Improvement Processes and Tools, including Process Mapping. Summary: The Global Process Owner (GPO) - Logistics & Warehouse Management (LWM) is a leadership role within the Global Logistics organization responsible for the overall strategy, design, policies, transformation, and standardization of business processes and related systems solutions for Logistics including Transportation Management and Warehouse Management in Distribution Centers and Production Plants.
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process improvement jobs Title: analyst Company: Kforce in Grayslake, IL
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