Sutter Gould Medical Foundation-posted 10 months ago
$62 - $78/Yr
Full-time
Sacramento, CA
Ambulatory Health Care Services

This position has a focus on Point-of-Care testing, and is responsible for coordinating all internal and external laboratory services performed as part of the specified point of care (POC) program sites. Responsible for validity of test results, result reporting, specimen handling, and maintenance of department POC and competency records. Will train staff at various sites. Assists in maintaining and continually improving the laboratory's Quality Management Program (QMP), to include monitoring, reporting and assessing performance-related information. Functions as a subject matter expert; advises on all aspects of the Lab's Quality Control Program, Process Management and External/Internal Assessments (i.e. proficiency testing and surveys/inspections). Investigates, reports and facilitates resolution of non-conforming events. Provides data and reports to support the quality review activities of the Medical and Operations Management teams, ensuring continual improvement of operational quality and service. Facilitates the design and validation of efficient workflow processes. Conducts, and participates in, quality-related meetings. Develops a variety of QMP documents (process maps/tables, procedures and forms) Supports regulatory compliance and accreditation readiness by coordinating or completing activities to fulfill requirements. Promotes a culture of quality by educating others. Facilitates complete and compliant management of records as applicable to assigned Lab section(s).

  • Coordinate all internal and external laboratory services for Point-of-Care testing.
  • Ensure validity of test results and result reporting.
  • Handle specimens and maintain department POC and competency records.
  • Train staff at various sites.
  • Assist in maintaining and improving the laboratory's Quality Management Program.
  • Monitor, report, and assess performance-related information.
  • Advise on Lab's Quality Control Program and Process Management.
  • Investigate and resolve non-conforming events.
  • Provide data and reports for quality review activities.
  • Facilitate design and validation of efficient workflow processes.
  • Conduct and participate in quality-related meetings.
  • Develop QMP documents such as process maps, procedures, and forms.
  • Support regulatory compliance and accreditation readiness.
  • Promote a culture of quality through education.
  • Graduate of an accredited Clinical Laboratory Scientist program.
  • CA Licensed Clinical Laboratory Scientist.
  • 5 years recent relevant experience.
  • Experience with training others preferred.
  • Demonstrated knowledge in quality systems, project management, and regulatory compliance.
  • Knowledge of CLIA '88 and California Business and Professional Codes.
  • Knowledge of quality practices in a clinical laboratory environment.
  • Well-developed analytic and software skills.
  • Ability to organize and prioritize job duties.
  • Ability to maintain confidentiality and follow standard practices.
  • Comprehensive benefits package.
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