Clinical Laboratory Quality Analyst
Clinical Laboratory Quality Analyst
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Job Description
Labcorp is seeking a Laboratory Quality Analyst to join our team at Troy Lab in Troy MI. 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: Flexible Schedule : Monday Friday 9am5:30pm
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 pleaseclick 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
- Associates degree in a Chemical or Biological science Clinical Laboratory Science Medical Technology or meet local regulatory (CLIA & State) requirements Bachelors degree is a plus
- 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 youre 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:
As an EOE/AA employer Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race religion color national origin gender (including pregnancy or other medical conditions/needs) 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. Additionally all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.
We encourage all to apply
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Required Experience:
IC
Employment Type
Full-Time
