Provides leadership in the areas of quality assurance, quality
control, quality-related training, and standardization compliance
within the laboratory. This position is also responsible for
project management activities as they relate to identified areas
within the laboratory requiring standardization to improve the
quality and/or efficiency of operations.
Document control - manage current versions of current procedures
Quality Indicators -- collect and report metrics
Proficiency Testing handling -- document evaluation review and
investigate trends and unsuccessful performance.
Internal Auditing -- Schedule, Audit, Report, document
corrective action and close audits.
Inspection readiness -- support lab team and work towards
constant compliance with regulatory requirements.
Quality Meetings -- schedule, provide agenda, conduct meetings
and report minutes.
Personnel Records -- review for completion, track and file.
Nonconforming events -- document incidents, assist with
investigations, root cause analysis, corrective action, preventive
action and measurement of effectiveness.
License/Certification/Education: Normally a B.A./B.S. Degree in
Medical Technology (Biological, Chemical, or Clinical Laboratory
1 year or more testing experience in a CLIA licensed clinical
Preferable leadership experience (lead tech or lab supervisor
Prior CAP inspection experience
Strong Communications (Oral and Written)
proficient a MS Office, such as Word and Excel
Shift 1 Schedule Monday through Friday: 8 AM to 5 PM (1 Hour
lunch)...flexible start tine if you want to start early