Phoenix, Arizona, USA
4 days ago
Clinical Laboratory Quality Analyst

Labcorp is seeking a Laboratory Quality Analyst to join our team at Phoenix, AZ. The Quality Assurance team provides vital support to the laboratories, senior management as well as our clients, and other Labcorp sites.  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. 

Work Schedule:  Monday - Friday 8:00 AM - 4:30 PM.

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 monthly and quarterly quality metric reports for clients and leadership using databases and crystal reports 

Assist staff with training in MasterControl, update and maintain all lab general and quality procedures, forms and associated documents 

Provide data for quality teams and support all Quality Improvement efforts 

Schedule and conduct QA audits and inspections of assigned departments/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  

Perform first level review of proficiency testing results 

Draft responses to regulatory complaints and inspection 

Stay current with all regulatory agency and proficiency test requirements 

Monitor the progress of implementation and subsequent use of MasterControl document management system  

Participate in monthly Quality meetings and compose minutes 

Serve as a resource on regulatory issues and compliance 

Perform administrative and clerical duties as needed 

Requirements 

Associate or Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, or Medical Technology  

Previous experience as a Medical Technologist/Technician or in a quality related position 

Prior experience in a clinical laboratory is highly preferred  

Familiarity with an electronic data management system is a plus (i.e. MasterControl) 

General knowledge of laboratory regulations (CAP/CLIA/ISO) and licensing requirements 

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 you're 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.

We encourage all to apply

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