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Highly experienced in Training & Development, Process Improvement, Strategic Recruitment Planning and People Management. Binding Minds, a diverse staffing company with expertise in Healthcare, Legal, IT recruitment, looking to hire an experienced Account Manager – Healthcare Staffing and join our expanding team in Bridgewater, NJ. We help our Healthcare clients with their staffing needs.
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Other responsibilities include participation in process tech transfer and incoming process changes, communicate the changes to applicable departments, and lead the process improvement projects at the site.
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Supporting the escalated requests, major incident management, RCA & RCCA. Identifying & implementing continuous improvement & automation opportunities. Experience with PowerShell, PowerShell Workflow and troubleshooting PowerShell ISE Direct Experience migrating email from Exchange on-premise/hosted to Exchange online through various migration methods (Cutover, Staged, Hybrid) Implementation of advanced functions of Office 365 Security and Compliance center - AIP, ATP, Mail flow rules management, Managing DNS records, Exchange online protection, SPAM & security controls.
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Managing and overseeing Systems Integration and AMS partners for the deployment of new capabilities and the enhancement/continuous improvement of processes, utilizing Product-Oriented Delivery and Agile methodology.
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The Vice President of Global Strategic Regulatory Operations (GRSO) reports directly to the Senior Vice President of Global Regulatory Safety and Biometrics (GRSB) and is a member of the GRSB Leadership Team. As such, this position has accountabilities for the sustained health, growth and continuous improvement of the GRSB organization, inclusive of developing effective partnerships with critical stakeholders across the BMS enterprise.
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We specialize in aluminum extrusion and fabrication, and we’re committed to delivering high-quality products through continuous improvement and advanced manufacturing techniques. The successful candidate will leverage Lean Principles, Six Sigma Methodologies, and Advanced Automation and Robotics to drive continuous improvement, enhance product quality, and increase operational efficiency.
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The Intelligent Automation Architect will work closely with cross-functional teams to identify opportunities for automation, design and implement solutions, such as automations for Clinical trial agreements, contract management, site management relates tasks, trial master file management, to streamline/speed up tasks and ensure their effective/secure utilization, faster completion, error/cost reduction and data quality improvement.
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Utilize various techniques such as ddPCR, Flow Cytometry, ELISA, Viability assay, and cell culture;Support ongoing EMPQ, cleaning and disinfection, and improvement of aseptic control. Utilize various techniques such as ddPCR, Flow Cytometry, ELISA, Viability assay, and cell culture;Support ongoing EMPQ, cleaning and disinfection, and improvement of aseptic control.
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As a Quality and Compliance Team Lead, you will serve as a liaison to key clients, where your leadership and expertise will contribute to the continuous improvement of our drug safety processes, regulatory and contract compliance, and overall patient safety.
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Experience working with external parties and/or cross-functional teams Responsibilities: Participation in process tech transfer and incoming process changes, communicate the changes to applicable departments, and lead the process improvement projects at the site.
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Enable savings and assurance of supply, manage savings leakage across downstream procurement processesAdminister continuous improvement projects initiated by the PSC team, embracing and furthering a spirit of adaptability and innovation in procurement operations.
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Applies continuous improvement tools to identify and close procedural and compliance gaps. Author, and approve protocol and reports in accordance with internal and external regulatory expectations (APS, Engineering, Tech Transfer.
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The Director leads performance improvement initiatives to improve clinical management of the continuum of care process, length of stay, denials management, and status of patients. The Director identifies improvement opportunities and facilitates process standardization to promote outcomes in alignment with the strategic and operational goals of Penn Medicine Princeton Medical Health by maximizing resource utilization and improving organizational efficiencies.
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TECHNICAL & BEHAVIORAL REQUIREMENTSTechnicalSkilled in design and execution of experimental test programsChemical Engineering skills & ability to define remodeling or technical improvement of pilot unitKnowledge of heavy oil upgrading technologyUnderstanding of design and operation of pilot plant testing equipmentFamiliarity with laboratory testing methodsKnowledge of SAP (or similar ERP system) and Customer Relation Management (CRM) program experience required.
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Certification(s) in Project Management (FPX, CAPM, or PMP) and/or Process Improvement (Lean Six Sigma). Experience with Supply Chain Systems (SAP, MES (PAS-X), eLIMs, OMP, OSI-PI Historian). Learn more at Janssen Biotech, Inc., one of the Janssen Pharmaceutical Companies of Johnson & Johnson, and Legend Biotech USA Inc., have entered into a global, strategic collaboration to develop, manufacture, and commercialize a chimeric antigen receptor (CAR) T-cell therapy.
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improvement job Title: coop Company: Ingredion in Montgomery, NJ
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