Lab POC and Compliance Coordinator

CURRENT BRONSON EMPLOYEES - Please apply using the career worklet in Workday.  This career site is for external applicants only.

Team Bronson is compassionate, resilient and strong. We are driven by Positivity which inspires us to be our best and to go above and beyond for our patients, for one another, and for our community. 

If you’re ready for a rewarding new career, join Team Bronson and be part of the experience.

The key responsibilities of the Lab Coordinator supporting Point of Care Testing (POCT), Quality and Compliance: 

• Oversee the day-to-day operations of Point of Care (POC) testing activities outside of the main laboratory. Coordinate work-related tasks to ensure testing is performed within acceptable safety and quality guidelines. Ensure that regulatory and compliance requirements are met. Understand all technical aspects of POC Testing including methodology and instrumentation. Function as expert advisor on POC testing methods and suggest and implement local applications.
• Facilitation of on-going laboratory compliance with clinical regulatory and accreditation requirements ie CAP, JC
• Facilitation of the lab’s quality management system (QMS) and quality initiatives

• Bachelor's degree from an accredited college including courses in biological science, chemistry, and mathematics

• Completion of Medical Laboratory Scientist program approved or accredited by the NAACLS

• Certification as a Medical Technologist-MT (pre 2004 certifications only) or Medical Laboratory Scientist-MLS from ASCP Board of Certification (BOC). All individuals who are certified (since January 1, 2004) must maintain ongoing certification as a MLS through completion of the required Competency Maintenance Program (CMP) from the ASCP (American Society for Clinical Pathology) BOC accrediting body

• All individuals must have completed certification OR be registry eligible and complete certification within one year of hire through ASCP, AMT or equivalent credential in Medical Laboratory Science or Medical Technology.

• All individuals who are newly ASCP certified after January 1, 2004 or newly AMT certified after January 1, 2006 must maintain ongoing certification

• 2 years of full-time experience in the clinical laboratory

• →Works in collaboration with all lab sections, pathologists, and other hospital departments to assure quality services are provides to all patients and customers
• →Assumes responsibility and assists with the coordination and management of Bronson Laboratory quality management system (QMS), related systems and processes
• →Facilitate documentation of laboratory non-conforming events. Manages data to promote process improvements and corrective actions
• →Apply and mentor use of process improvement tools
• →Facilitate documentation of quality metrics and indicators, assessments and action plans for continual improvement
• →Facilitates internal PDSA and risk audit process to assess effectiveness of corrective actions

• →Current driver’s license in the state of Michigan and excellent driving record is required.
• →Driving your own vehicle on a regularly scheduled basis to perform business on behalf of Bronson is required for this position and will require successfully pass of MVR check after an offer of employment has been made but prior to the employee’s start date. Proof of valid auto insurance on that vehicle that will be driven while on duty for Bronson is required. It is the employee’s responsibility to submit auto. insurance renewals before current coverage expires to their supervisor. It is also the employee’s responsibility to update their auto insurance coverage with Bronson if a different vehicle will be driven to perform business on behalf of Bronson.
• →Must be able to operate and perform computer program functionality associated with documentation and record keeping in the department.
• →Must demonstrate a degree of independent judgment, problem solving along with critical thinking 
• →skills consulting with the manager when appropriate.
• →Must be able to move from task to task, maintaining quality and efficiency.
• →Shows dignity and respect to patient, family and team members.
• →Communicates and shares information with providers and team members, both verbally and written.
• →Treats team members as valued partners.
• →Demonstrates teaching, coaching and mentoring skills.

• Facilitates laboratory clinical compliance with regulatory standards including CAP, CLIA, FDA and TJC
• Directs activities of laboratory testing within and outside of the laboratory maintain regulatory compliance with CAP, CLIA, FDA, TJC and other standards as applicable

Work which produces high levels of mental/visual fatigue, e.g., interactive and repetitive or small detailed work requiring alertness and concentration for sustained periods of time, the operation of and full attention to a personal computer or CRT between 40 and 70 percent of the time.

The job produces some physical demands. Typical of jobs that include regular walking, standing, stooping, bending, sitting, and some lifting of light weight objects.

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