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Clinical Laboratory Quality Analyst

Clinical Laboratory Quality Analyst

LCH Lab. of America HoldingsWichita, Kansas, USA
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LabCorp is seeking a Laboratory Quality Analyst / Point of Care Coordinator to join our team in Wichita KS. The Quality Assurance team provides vital support to the laboratories and senior management. The Quality Analyst will be responsible for supporting projects and activities related to quality assurance quality improvement quality training and other responsibilities of the Quality Assurance department. The Quality Analyst allows the laboratory to provide quality results to our providers and patients which increases customer satisfaction and solidifies loyalty for our company. They will manage point of care instruments competencies quality control documenting and reagent / supplies for units performing various types of bedside testing.

Work Schedule : Monday-Friday 8 : 00am-4 : 30pm

Benefits : Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including : Medical Dental Vision Life STD / LTD 401(k) Paid Time Off (PTO) or Flexible Time Off (FTO) Tuition Reimbursement and Employee Stock Purchase Plan. Casual PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information please click here.

Job Responsibilities :

  • Provide data for quality teams and support all Quality Improvement efforts
  • Schedule and conduct regular QA audits and inspections of assigned departments and facilities and perform audit reports
  • Ensure complete and accurate readiness for all inspections and maintain all necessary documents
  • Participate in regulatory and accrediting agency inspections when needed
  • Draft responses to regulatory complaints and inspection
  • Stay current with all regulatory agency and proficiency test requirements
  • Participate in monthly Quality meetings and compose minutes
  • Serve as a resource on regulatory issues and compliance
  • Perform administrative and clerical duties as needed
  • Provides guidance and support to assigned staff performing point of care. Creates and / or assists with training and ensures appropriate stock of reagents quality control materials etc.
  • Monitors competencies and is available for follow up when lock out occurs.
  • Monitors middleware for inappropriate barcode scanning testing and resulting errors and reports as appropriate.
  • Oversees and audits analyzer / cartridge failures and arranges for service or replacements.
  • Develops new POC test setups which may include project management vendor and Laboratory Information Services representation and validation of new tests. Authors policies.
  • Provides administrative technical and educational guidance for all testing performed. Ensures compliance with all regulatory agencies and accreditation standards with regards to safety and POC testing for all system laboratory sites.
  • Provides guidance and leadership to others responsible for POC functions across the system or multiple departments.
  • Reviews analyzes and reports on POC testing quality control and compliance data. Compiles monthly and annual compliance and incidence report summaries.
  • Acts a resource for the evaluation implementation and monitoring of all new POC testing.

Requirements :

  • Bachelors degree in a Chemical or Biological science Clinical Laboratory Science or Medical Technology
  • 2 years experience as a Medical Technologist in core lab setting required
  • Prior experience in a quality related position preferred
  • Familiarity with an electronic data management system is a plus (i.e. MasterControl)
  • General knowledge of laboratory regulations (TJC / CLIA / FDA / FACT) and licensing requirements
  • ASCP certification is preferred
  • Strong understanding of audit related requirements and procedures
  • Working knowledge of quality assurance / quality management best practices
  • Excellent analytical critical thinking and problem solving skills
  • Strong communication skills; both written and verbal
  • High level of attention to detail with strong organizational skills
  • Ability to work independently and within a team environment
  • Strong computer skills with proficiency with MS Office programs

    • If youre looking for a career that offers opportunities for growth continual development professional challenge and the chance to make a real difference apply today!

    Labcorp is proud to be an Equal Opportunity Employer :

    Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race religion color national origin sex (including pregnancy childbirth or related medical conditions) family or parental status marital civil union or domestic partnership status sexual orientation gender identity gender expression personal appearance age veteran status disability genetic information or any other legally protected characteristic. A dditionally all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

    We encourage all to apply

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    Required Experience :

    Key Skills

    Gas Chromatography,Laboratory Experience,Archival Standards,ELISA,Test Cases,Analytical Chemistry,Quality Assurance,Spectroscopy,Quality Control,cGMP,Selenium,Western Blot

    Employment Type : Full-Time

    Experience : years

    Vacancy : 1

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    Laboratory Laboratory • Wichita, Kansas, USA