Quality Auditor

Labcorp•Saint Paul, MN

13d•$72,000 - $88,000

About The Position

Labcorp is seeking a Laboratory Quality Auditor to join our team in St. Paul, MN . The Quality Assurance team provides vital support to the laboratories, senior management as well as our clients, and other Labcorp sites. The Quality Auditor 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 Auditor allows the laboratory to provide quality results to our providers and patients, which increases customer satisfaction and solidifies loyalty for our company. Pay Range: $72,000 - $88,000 annually All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data. Work Schedule: Monday - Friday, dayshift 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. 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. For more detailed information, please click here .

Requirements

Bachelors degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements
5 years of previous experience as a Medical Technologist/Technician or in a quality related position
ASQ Certified Quality Auditor (CQA) or equivalent certification is required or must be obtained within first 12 months.
Additional certifications and specific training may be required depending upon primary responsibility (e.g., RQAP-GLP, CMQ/OE, ISO, FDA GxP)
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

Nice To Haves

Prior experience in a clinical laboratory is highly preferred
Familiarity with an electronic data management system is a plus ( i.e. MasterControl )

Responsibilities

Maintain competency and understanding of quality requirements for laboratory accreditation agencies, including CAP/CLIA, SAMHSA, NYSDOH, and others
Plan and conduct the internal audits of the technical activities of the Clinical and Forensic Laboratories
Monitor the laboratory to assure laboratory management that equipment, methods, practices, records, controls, SOPs and policies are in compliance with regulations and accreditation requirements
Monitor/audit the performance of critical/key laboratory vendors, as needed
Plan and conduct internal audits of administrative departments, including IT/LIS, Facilities/Biomed, etc. to assure management that practices, records, controls, and SOPs are in compliance with regulations and accreditation requirements
Report all findings to management through internal audit reports
Follow-up on corrective/remedial actions to assure appropriate actions were taken and were effective
Aid directors, managers, and supervisory personnel in preparing for inspections.
Actively participate in all external inspections and audits, as directed
Follow the direction of the Division Quality Director to maintain the overall Quality Management System