• Dialysis Charge Registered Nurse - RN

    Fresenius Medical Center (Rochester, NY)
    …DUTIES AND RESPONSIBILITIES:** + Responsible for supporting and driving Organization quality standards through meeting regulatory requirements and the practice ... facility equipment and technology, including but not limited, patient monitors, defibrillators, medical recording devices and computers. + Maintains a clean,… more
    Fresenius Medical Center (07/05/25)
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  • Nursing Assistant I - Medical Inpatient 2

    Bassett Healthcare (Cooperstown, NY)
    …the population we serve, and our communities, achieve optimum health and enjoy the best quality of life possible. What you'll do The Nursing Assistant (NA) I is a ... indirect patient care within their scope of practice, supporting patients, nursing and medical care teams. The care delivered is in collaboration and under the… more
    Bassett Healthcare (08/01/25)
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  • Sr. MES Opcenter OR Camstar Consultant - Remote

    Cognizant (Albany, NY)
    …**Opcenter Technical:** A dynamic professional with proven expertise in Siemens Opcenter Medical Devices / Camstar application in Manufacturing Execution domain. ... cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Understand the… more
    Cognizant (07/18/25)
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  • Director, Clinical Operations

    Bausch + Lomb (Albany, NY)
    …Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/ Device Safety, and Clinical ... provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input...ICH, GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,… more
    Bausch + Lomb (06/07/25)
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  • Senior Technical Project Manager, SaMD

    Oura (New York, NY)
    …if you have: + 5+ years of experience working in a regulated environment under a medical device Quality Management System (21 CFR 820 or ISO 13485:2016) as ... the applicable standards and regulations governing the development of medical device software at Oura. This role...seeking a candidate with a strong personal drive of quality excellence and motivated by the desire to deliver… more
    Oura (08/15/25)
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  • Radiology Technologist: Azura

    Fresenius Medical Center (New York, NY)
    …for patient medical records and state regulations. + Provides outstanding quality of patient care by supporting and driving the organization's quality ... regulatory requirements and the practice of Continuous Quality Improvement (CQI), including use of CQI tools. +...and facility specific action plans to achieve the organization's quality standards. + Ensures medical records are… more
    Fresenius Medical Center (06/14/25)
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  • Surgical Technologist: Azura

    Fresenius Medical Center (New York, NY)
    …outstanding quality of patient care by supporting and driving USV quality standards through meeting regulatory requirements and the practice of Continuous ... quality goals and facility specific action plans in order to achieve USV quality standards. + Maintains integrity of medical records and other USV… more
    Fresenius Medical Center (06/14/25)
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  • Sales Representative - Specialty Medical

    Cardinal Health (Albany, NY)
    …including medical /surgical, copiers, payroll solutions, information) preferred + Medical Device industry experience preferred + Excellent phone, written, ... businesses. We offer industry expertise and an expanding portfolio of safe, effective medical products that improve quality , manage costs and reduce complexity.… more
    Cardinal Health (07/20/25)
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  • Coordinator, Point of Care Testing - Laboratory…

    Guthrie (Binghamton, NY)
    Position Summary: Position provides laboratory technical support and regulatory consultation for the Point of Care Testing Program (POCT) and assists with ... with inpatient staff to coordinate: POCT training and proficiency testing, device implementation and upgrades, POCT reagent inventory, health information system and… more
    Guthrie (08/08/25)
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  • Complaint Management Specialist

    ManpowerGroup (Medina, NY)
    …a cGMP related industry or in a clinical setting. + Strong knowledge of the FDA Quality System and Medical Device Reporting regulations (21 CFR 803, 806, ... Complaint Management Specialist, you will be part of the Quality Assurance department supporting the Product Surveillance team. The... execution. + Gain experience in complaint handling and regulatory compliance within the medical device more
    ManpowerGroup (08/20/25)
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