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Ensures compliance within guidelines set forth by regulatory agencies (DPH, ERISA etc.) Assists in clinical manager’s and scheduling coordinator in appropriate coverage based on census, skill mix, geographic location, patient need and clinical capacity.
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Interface with multiple departments at multiple locations (Production Group, Quality Control, Quality Assurance, Research Products, Operations and Logistics) and external consultants to ensure compliance with the company's Quality Management System, cGMP, and ISO standards.
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Canvasser - outside - inside - call center - entry level - automotive sales - luxury car - used car - medical - dental - pharmaceutical - solar - industry - brewery - agriculture - vacation - travel - insurance - mortgage servicing - mortgage processing - real estate - retail - customer service - dealerships - collections - startups - creative marketing - SDR - canvass - sales - construction - marketing - food service - canvassing- outdoor sales - appointment setter.
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Maintain required documentation according to DDS, DMH, MassHealth, HUD, DPH, CARF and all applicable regulatory standards as well as Bridgewell policies and procedures. Provide services to individuals according to DDS, DMH, MassHealth, HUD, DPH, CARF and all applicable regulatory standards, as well as Bridgewell policies and procedures.
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Through research, education, clinical practice and community partnerships, we are committed to the mission of advancing health, providing each person the best care, in the right place, at the right time, every time.
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Under supervision of the Director of Clinical Services, the Acquired Brain Injury (ABI) Clinician/Clinical Rehabilitation Specialist contributes as a member of a multi-disciplinary team supporting the community-integrated rehabilitation of adults with brain injuries.
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Advanced scientific degree and/or preferred 5+ years of pharmaceutical or biotechnology experience as healthcare sales / MSL / HCP / nurse. BMS is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives.
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Experience with Export/Import Compliance procedures and regulations. Its 185,000 employees enable the company to operate at the edge of known science as they imagine and deliver solutions that push the boundaries in quantum physics, electric propulsion, directed energy, hypersonics, avionics and cybersecurity.
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Monitors workplace activities to ensure compliance with company policies and government regulations. Shaw's Distribution Center in Methuen, MA, an Albertsons Company, is at the forefront of the revolution in retail.
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The mission of Advanced Technology is to develop and mature key technical discriminators through Contract Research and Development (CRAD) with our Science and Technology (S&T) customers, such as DARPA and Office of Naval Research (ONR.
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The Durable Medical Equipment (DME) Coordinator "Coordinator" is primarily responsible to ensure the ordering and securing of DME and other medical supplies for the patients at GLFHC is timely, efficient, and meets payer and other regulatory guidelines.
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Monitor changes in the business and regulatory environment and assess their impact on SOX compliance. Prior SAP GRC experience required; experience with SOX compliance software/tools is a plus.
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BlueTriton Brands, Inc. (BlueTriton) is a water and beverage company in North America that produces and distributes a portfolio of brands of spring water, purified water, and other beverages, which include Poland Spring, Deer Park, Ozarka, Ice Mountain, Zephyrhills, Arrowhead, Origin, Saratoga, AC+ION, Pure Life, BEAU, and Splash Refresher.
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Safelite is more than just an auto glass company. We're known as an auto glass company. Company Name: Safelite. Safely operate a company vehicle and company-issued tools utilized throughout the workday.
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Perform radiation safety duties to SOFIE Radiation Compliance/Environmental Health and Safety Program standards to ensure compliance with all regulations under the Corporate and site RSO. § Ensure compliance with all procedures and regulations within the site under the Quality Assurance program as applicable, including participating in exception document reporting (e.g. deviations, corrective and preventative action plans, out-of-specifications, etc.
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