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Job Description & Requirements Specialty: Electrophysiology Technician Discipline: Allied Health Professional Start Date: ASAP Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel MedPro Healthcare Staffing , a Joint Commission-certified staffing agency, is seeking a quality EP Tech for a contract with one of our top healthcare clients.
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Current compliance with Continuing Medical Education (CME) requirements for specialty (ies) as appropriate. We are innovating value-based care and leveraging integrated applications, population insights and staffing expertise to ensure all patients have access to high-quality, connected care services that provide better outcomes at a reduced total cost of care.
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The Coding Quality Auditor is responsible for monitoring compliance with applicable clinical documentation to support coding and billing regulations to insure appropriate reimbursement and to support public reporting and various initiatives as directed by Hackensack Meridian Health (HMH) Network.
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Reporting to the Head of US Quality and Regulatory Compliance, you will be part of a corporate level team responsible for improving the evaluation and management of contract manufacturers, packagers, warehouses/distributors, laboratories used to deliver foods, dietary supplements, cosmetics, OTCs, and medical devices.
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Adhere to standards and direction driven by global IS Quality team Supporting the IT components of any CAPA opened by the Quality Assurance (QA) team Support both Aptar IS DB team and Instrument vendors on database management, including any supported remote databases or local workstation databases Ensure local inventory documentation is up to date and includes documentation to support compliance needs around backups, OS level, patch level, software version, etc.
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Maintains established departmental policies and procedures, objectives, quality assurance program, safety, environmental, and infection control standards. Collaborates with all members of the health care team to complete MDS/care planning in compliance with regulatory agency requirement.
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Evaluates the effectiveness of Contractors’ quality systems by leading effective audits for cGMP compliance, issuing audit reports, managing Contractor response adequacy and timeliness; determining system improvements.
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Experience with HIPAA compliance, coding, charging and billing. The Associate Director, Payer Reimbursement (AD) manages and oversees the output and quality of all payer accounts receivable under their scope and is expected to collaborate with their payer managers and the Senior Director of Revenue Realization to identify strategies for performance improvement on a weekly, monthly, and annual basis.
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We have a diverse range of portfolios throughout the ZEISS family in segments like, Industrial Quality & Research, Medical Technology, Consumer Markets and Semiconductor Manufacturing Technology.
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As a Senior Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. Where applicable, perform job responsibilities in compliance with cGMP/GLP and all other regulatory agency requirements.
$107,600 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job Title: Quality Assurance CoordinatorJob DescriptionThe Quality Assurance Coordinator is responsible for perpetuating Enterprise-wide Quality and Regulatory compliance and continuous improvement.
$25 - $32 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As a Clinical Care Manager for our Licensed Home Care Service agency, you will play a crucial role in ensuring the delivery of high-quality home care services in compliance with the regulations set by the New York State Department of Health.
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Build Quality into all aspects of your work by maintaining compliance to all quality requirements. Read, understand and follow all cGMP and cGTP documentation for Quality System Functions (SOPs,WIs.
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Reports to: Administrative Director ofLaboratoriesPosition SummaryThe Supervisor is responsible for coordinating and directing all activities of the Chemistry and Immunology laboratories to achieve maximum quality of testing and compliance with all requirements by regulatory agencies.
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SummaryThe Supervisor is responsible for coordinating and directing all activities of the Chemistry and Immunology laboratories to achieve maximum quality of testing and compliance with all requirements by regulatory agencies.
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quality compliance jobs in Northvale, NJ
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