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Perform site safety assessments and compliance management reviews and report on EHS performance and tactical and strategic improvement planning with general contractors and sub-tier contractors both for Aligned construction projects and data center operations.
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The Director will ensure the proper preparation and coordination of resources needed to achieve regulatory compliance related to the CMS COP Quality Assessment and Performance Improvement (QAPI) Plan and QAPI Annual Evaluation, and The Joint Commission standards, Co-chaired Quality Committee related to performance improvement, to include the collection, analyses, reporting and on-going monitoring of quality and safety data needed to meet accreditation requirements.
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Oversee medical necessity chart review for all federally funded orders and conduct re-training as necessary for Sales and internal staff (ISR), to ensure performance improvement. to ensure accurate and timely responses as well as implement necessary changes to policies and procedures for performance improvement.
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The Supply Chain Director is responsible for leading and aligning all supply chain & procurement activities across the firm’s offices, implementing data driven procurement strategies, implementing a centralized shared services model of procurement professionals, optimizing consistent processes, negotiating equitable supplier terms, developing effective supplier partnerships, reducing supply chain spend, and driving project and financial performance improvement.
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Implement and execute strategic initiatives aimed at injury prevention, risk management, and general safety performance improvement. Oversee and monitor regulatory compliance in air permitting, storm water management permits and plans, spill prevention plans, hazardous waste management, land permitting and maintenance, water treatment, injection well permitting and maintenance.
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Identify opportunities for continuous improvement, optimize and ensure procurement process compliance, and help scale the supply chain function in a fast-paced growth environment by leveraging automation.
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The Risk Management and Regulatory Compliance Coordinator provides leadership for safety, accreditation and regulatory activities through relationship with hospital administration and leadership, medical staff leadership, physicians, nurses, and ancillary and allied health departments to improve knowledge and performance for hospital safety, performance improvement and quality initiatives.
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Department LABORATORY ANIMAL RESOURCES (IN-LARS-IUINA) Job Summary Performs experienced animal husbandry and/or assists with animal clinical care and other related tasks (such as compliance/regulatory functions, process improvement, medical evaluations, supportive medical treatments and procedures, surgery support, diagnostic testing, checking protocols, maintaining inventory supply, performing audits/inspections, outcome tracking, cost analysis, etc.
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Aid in the quality management of the Drug Safety system, including ensuring department standards, training requirements, performance monitoring, and implementing continuous improvement actions.
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Supports the organizations ISO-9001 / AS9100 certification; reports key performance measures, performance levels and trends at quarterly business reviews and other meetings as required; leads small teams through continual improvement efforts to address internal or external corrective actions.
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Quality Management: Facilitates the preparation of formal corrective and prevention action initiatives including documentation for Root Cause Analysis (RCA), Failure Effect Mode Analysis (FEMA), and any resulting Performance Improvement Plans (PIP.
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Lead and coordinate efforts to implement risk mitigation, injury prevention and EHS&S compliance initiatives, develop and execute tactical strategic plans to improve site EHS&S performance to continually improve overall EHS&S performance.
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As a Sterile Processing Technician, the technician will also assist in the eduation and training of other staff (e.g., new hires) with respect to quality assurance, performance improvement, and departmental compliance.
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The Supplier Quality Engineer will be responsible for executing various supplier quality engineering related activities such as Compliance, Process, and Product Audits, MRB, FAI Witnessing, Review and Sign off, Problem Solving, Corrective and Preventive Actions, Supplier Performance Reporting and other Quality Improvement Activities.
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These solutions include innovative, creative, and responsive training, organizational development, change management, and strategic performance improvement services. Design, develop, and document instructor-led, paper-based, and responsive technology-delivered curricula and performance support solutions.
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