Location
Wildwood GA
Date Posted
4/11/2022
Job Type
Full-Time Regular

Division Quality Coordinator- Med Tech

Candidate must reside or be willing to relocate to the Fort Lauderdale market

Our client offers an amazing compensation package with industry leading incentives, great benefits and the opportunity to live and work in one of the most beautiful, affordable and exciting coastal communities in the United States!

We have an exciting opportunity for you to join our Integrated Regional Laboratories (IRL) executive team which is part of the nation's leading provider of healthcare services. This role will support 4 Divisions which includes 80+ healthcare facilities and 3 reference labs in the state of Florida. This role will require travel within the state of Florida and office is located at the Corporate Office in Fort Lauderdale.

Job Summary

Support 14 hospitals in the East Florida Division supervising and administering the Division Laboratory Quality Assurance programs under the direction of the IRL Quality Director, Division Director and medical directors to meet patient care and regulatory agency requirements. Consult and lead the quality initiatives and strategies and build strong relationships with division key stakeholders to include medical directors and administrators. Monitor all regulatory agency inspection preparedness activities. Facilitate and build strong relationships with department leaders to implement new programs, monitor performance, collect and evaluate performance data and root/cause analysis, develop corrective action plans, assist in the training and education of personnel regarding quality activities. Support the Quality and Division Directors in achieving department goals for service, quality, regulatory compliance, financial performance, patient satisfaction, healthy work environment, and integration of intra and inter-departmental activities. Hybrid role with about 40% travel with limited overnight travel

Position Qualifications:

    Education/License/Certification:
    • 4 year Bachelor’s degree in Medical Technology
    • State of Florida Supervisor’s license in all specialty areas or the ability to obtain
    Experience/Skills:
    • 3-5 years of quality assurance and regulatory agency compliance experience
    • 1-3 years in a clinical laboratory setting with quality assurance and/or point-of-care testing
    • Strong communicator and relationship builder
    • Excellent time management
    • Flexible and adaptable
    • Ability to lead by persuasion
    Click here to apply online