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Responsible for service parts management for United Imaging USA parts network, including planning, scheduling, QMS compliance, risk mitigation and vendor management. Handles Return Material Authorization (RMA) process to include tracking, contacting (internal) customers regarding returns, metric reporting, disposition with QA and coordinating with freight companies.
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Reviews pertinent legal, approval, and budget documents at each step of the internal audit and closing process to ensure compliance with approved terms, including, but not limited to, project reconciliations, agendas, purchase and sale agreements, leases, title commitments, surveys, site plans, settlement statements, deeds, development agreements, easements, covenants, restrictions, permits, environmental site assessments, geotechnical studies, and various legal memoranda.
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Displays integrity and professionalism by adhering to Life Care's Code of Conduct and completes mandatory Code of Conduct and other appropriate compliance training. Patience, tact, cheerful disposition, and enthusiasm as well as willingness to handle difficult patients.
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The Specialist, Manufacturing Technical Investigations and Analytics (MTIA) will work collaboratively across departments to ensure a state of compliance exists within Vertex Manufacturing Center (VMC), manufacturing, facilities and warehouse operations.
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This includes regular and frequent inspection of equipment and facilities, and handling/disposition of hazardous waste. Work closely with production workers/supervisory personnel in evaluating production activities and creating a safe work environment; while looking for continuous improvement opportunities Assuring regulatory compliance in areas of policies, training, equipment and environmental control Evaluation and monitoring of personal protective equipment Assist with incident investigations Coordination of emergency safety drills Your Professional Experience Should Be.
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Monitor pricing and markdown accuracy ensuring inventory disposition are in compliance with Kohl's Best Processes. Oversee store Cash Office, Service Desk, and Building Safety standards are maintained and take appropriate action when necessary.
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Batch record review and product disposition. The Quality Assurance Manager will ensure compliance with current Good Manufacturing Practices (cGMP) as they pertain to the local regulation and exporting countries regulation as applicable (such as FDA, MHRA, EMA, Health Canada.
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G.S. Precision is committed to Equal Opportunity Employer (EOE) and to be in compliance with all Federal, State and local laws that prohibit employment discrimination on the basis of race, color, age, natural origin, ethnicity, religion, gender, pregnancy, marital status, sexual orientation, citizenship, genetic disposition, disability or veteran's status or any other classification protected by State/Federal laws.
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Job Responsibilities:Reviews medical record documentation and accurately assigns appropriate ICD-10 diagnoses and procedure codes, leading to the assignment of the correct Medicare Severity-Diagnosis Related Group, (MS-DRG) or All Patient Refined Diagnosis Related Group, (APR-DRG.) The Inpatient Coding Specialist is responsible for verification of the patient's discharge disposition and to ensure the appropriate present on admission, (POA) indicators are assigned to each code.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The QA Reviewer is responsible for a variety of Quality activities to ensure compliance with applicable quality objectives and regulatory requirements in the cGMP Quality organization. Thorough knowledge of and competence in quality processes, including but not limited to material disposition, deviations, investigations, and CAPA management.
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Records checking and compliance results on paperwork using standardized markings and formattingWorks with supervisor to identify and correctly, document, resolves and/or disposition OS&D scenariosInteracts with supervisors and leads to help identify trends, processes, or vendor/client specific issues that need to be addressed.
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Avantor's Legal Department is seeking a Senior Counsel, Litigation and Investigations (Commercial) to support client groups within Avantor's enterprise, reporting to Senior Vice President, Deputy General Counsel, Global Litigation and Compliance.
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Direct a team with responsibilities for quality engineering activities (e.g., process and test methods validations, product transfer, process improvements, non-conformance investigation, corrective action, product disposition, complaint analysis, risk management) with overall responsibility of developing quality processes, staffing, planning, budgeting, aligning priorities, performance management, and working through managers to achieve results.
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In the event that we enter into, or intend to enter into, a transaction that alters the structure of our business, such as a reorganization, merger, acquisition, sale, joint venture, assignment, consolidation, transfer, change of control, or other disposition of all or any portion of our business, assets or stock, we will share personnel personal information.
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Perform value engineering to reduce DOE’s real property asset ownership costs and perform cost benefit studies to evaluate alternate packaging and loading to reduce cost of waste disposition. Serves as Design Authority Develop designs that are recognized and generally accepted good engineering practices in compliance with regulatory and permitting requirements, maintaining configuration control of all design documentation, including as-built drawings.
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