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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
$2,071 a weekFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Adaptability and Resilience: The additive manufacturing industry can be subject to fluctuations in demand, technological advancements, and regulatory changes. Safety and Compliance: A thorough understanding of safety protocols and regulatory compliance related to hazardous materials handling is essential.
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Provide oversight to manage and strengthen creative donor-centered marketing strategies as the key communications tool for the planned giving within Development and Alumni Affairs (, Corporate Relations, Foundation Relations, Donor Experience, Prospect Development and Alumni Relations), as well as other university units, to ensure coordination with major and planned giving prospects and donors.
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Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements. Ensure laboratory is compliant with corporate, state and federal regulatory requirements (CAP, CLIA, State, ISO, etc) related to personnel safety and quality of laboratory testing as well as professional conduct.
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The ETAR Risk Specialist Sr., conducts modeling, development, research and analysis to ensure appropriate modeling techniques and assumptions deployed in the company’s trading and risk systems, in order to adequately capture the company’s market and counterparty credit risk, and keep ongoing compliance with model risk management requirements, and regulatory requirements.
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Maintain a safe work environment and wear appropriate personal protective equipment Requirements:Bachelor's degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements.
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Job Duties/Responsibilities:Responsibilities are interchangeable within job titles of medical laboratory scientist (MLS), medical technologist or clinical laboratory scientist. MICRO LAB MED TECH WITH PLATE READING EXPERIENCE Perform routine medical laboratory tests for the diagnosis, treatment and prevention of disease.
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Minimum 0-2 years of clinical laboratory testing experience is required. Perform and document preventive maintenance and quality control procedures. Consult with a pathologist to determine a final diagnosis when abnormal cells are found.
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Location: Various locations across Michigan As a Corporate Secretary you will manage the company s corporate records ensure compliance with statutory and regulatory requirements and handle corporate governance matters.
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Experience with Roche and Meditech would be greatly appreciatedASCP- not required but strongly preferred. to Perm. Perform routine medical laboratory tests for the diagnosis, treatment and prevention of disease.
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The CISO is responsible for identifying, evaluating and reporting on legal and regulatory, IT, and cybersecurity risk to information assets, while supporting and advancing business objectives. Work with business units to ensure that all information owned, collected or controlled by or on behalf of the company is processed and stored in accordance with applicable laws and other global regulatory requirements, such as data privacy.
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STATUS: Full time DIVISION: Student Affairs REPORTS TO: Dean of Students SUPERVISES: N/A FLSA STATUS: Exempt Position Description The College for Creative Studies is seeking an experienced professional for the position of Director of Civil Rights, Equity, and Title IX. Reporting directly to the Dean of Students, this position serves as the principal institutional official responsible for leading efforts across the College to ensure compliance with federal Title IX and civil rights policies.
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Monitor, operate and troubleshoot instrumentation to ensure proper functionality. Job Responsibilities: Set up, adjust, maintainand clean medical laboratory equipment. Demonstrate the ability to make technical decisions regarding testing and problem solving.
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Perform routine and complex technical procedures and functions according to departmental Standard Operating Procedures. Report accurate and timely test results to deliver quality patient care. Analyze the results of tests and experiments to ensure conformity to specifications, using specialmechanical and electrical devices.
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Leads Sarbanes-Oxley controls testing and other required regulatory testing (e.g., North American Electric Reliability Corporation Critical Infrastructure Protection (NERC-CIP), etc.) Experience with business operations systems, cyber security, network/database engineering, controls/risk assessments, information security and privacy, and/or regulatory compliance.
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regulatory affairs jobs Title: travel in Detroit, VA, New Jersey
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