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Labcorp Quality Analyst for COVID Department in Research Triangle Park, North Carolina

LabCorp is seeking a Laboratory Quality Analyst to join our COVID team in RTP, NC. 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.

The schedule for this position will be 1st shift (Monday-Friday 8:00am-5:00pm)

Job Responsibilities:

  • Provide monthly and quarterly quality metric reports for clients and senior 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 regular QA audits and inspections of assigned departments and 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

  • Requires a Bachelor's Degree in Biology, Chemistry, or related scientific discipline

  • Minimum 2 years of experience assisting with or managing a quality management system in a regulated environment. Previous clinical laboratory highly desired. OR

  • Minimum 2 years of clinical laboratory experience with experience and familiarity with quality processes

  • Previous experience 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

Shift

1

Schedule

1st shift (Monday-Friday 8:00am-5:00pm)

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

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