Clinical Laboratory Quality Analyst

Labcorp • Birmingham, AL

3d • Onsite

About The Position

Labcorp is seeking a Quality Assurance Analyst to join our team in Birmingham, AL. Work Schedule: Monday - Friday, 8:00 am - 5:00 pm 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 At Labcorp we have a passion for helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step! Join us and discover a path filled with opportunities for growth, continuous learning, professional challenges, and the chance to truly make a difference. Apply today!

Requirements

• Associate’s degree in a Chemical or Biological science, Clinical Laboratory Science or Medical Technology
• 5 years of clinical laboratory testing experience or in a quality related position
• In lieu of education requirements listed above, non-traditional degrees with applicable science credits that meet CLIA standards may meet education requirements
• General knowledge of laboratory regulations (CAP/CLIA/ISO) and licensing requirements
• Understanding of laboratory operations as well as policies and procedures
• Basic understanding of audit related requirements and procedures
• Working knowledge of quality assurance best practices and procedures
• Excellent analytical, critical thinking and problem solving skills
• Ability to work independently and within a team environment
• Proficient with computers; Familiarity with laboratory information systems
• High level of attention to detail along with strong communication and organizational skills
• Ability to handle the physical requirements of the position
• Able to pass a standardized color blindness test
• Flexibility to work overtime or other shifts depending on business needs

Nice To Haves

• Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science or Medical Technology
• 3 months or more of experience in a clinical laboratory
• Familiarity with an electronic data management system is a plus (i.e. MasterControl)
• Experience working in a high volume laboratory environment

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

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.
• Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.
• Employees who are regularly scheduled to work a 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree
• Number of Employees: 1-10 employees