Quality Specialist II

Under the directive of the Quality Supervisor, the Quality Specialist is responsible for planning and coordinating all of the functions within the scope of Quality. This includes but is not limited to reviewing, interpreting and maintaining the Quality Control Program, arranging for and conducting quality audits, assisting with and reviewing Method/Instrument Validations, coordinating proficiency survey programs, writing and reviewing standard operating procedures, maintaining compliance with all regulatory standards to ensure that services are of the highest quality, recognizing results or problems, assisting Laboratory with performance improvement/quality management monitors, and ensuring the laboratory is adhering to all regulatory requirements.

• →Bachelors of Science in Medical Technology.
• →4 or more years of CLIA laboratory or related experience working as a Medical Technologist. Bench areas of experience Urinalysis, Special Coagulation, Hematology, Toxicology, Serology, Chemistry, etc.
• →Will consider a Medical Lab Technician with 8+ years of experience working as a generalist in a CLIA lab.
• →ASCP or other national certification preferred. ASQ Certification a plus.
• →Up to 30% Domestic Travel

• Medium work of lifting up to 50 pounds and/or carrying objects weighing up to 25 pounds.
• Responsible for lifting, carrying, pushing, and pulling objects.

• Work requires sitting, standing, and/or walking for periods of up to four hours.
• Work requires contact with water (hand washing and cleaning), biohazardous body fluids, and hazardous chemicals.
• Work is varied in nature with sufficient noise and interruptions to cause distraction and stress.
• Work requires close attention to detail and accuracy.
• OSHA risk factor: Category 1