QA/QC Specialist - IGM Clinical Admin
On-site · Columbus, Ohio, United States
Job Summary
Coordinates quality control, regulatory compliance (CAP/CLIA, NYS testing requirements), inspection readiness, and education within the Institute for Genomic Medicine. Serves as General Supervisor per CAP/CLIA guidelines and Lab Supervisor per New York State testing guidelines as applicable. Leads group training for education of lab staff in performing quality control and quality assurance responsibilities. Coordinates the IGM Quality Monitoring program. Prepares reports, investigates incidents and deficiency reports, and solves problems regarding deviations from established procedures and processes. Tracks and reviews laboratory documentation regarding training and competency, education, and use and maintenance of equipment. Facilitates the creation, updates, activation, and distribution of Standard Operating Procedures. Collaborates with supervisor and manager to coordinate process improvements and implement new workflows. Facilitates and leads workgroups and projects. Performs in-depth troubleshooting and problem-solving, predicting and avoiding problems using information from quality control checks and recommending improvements. Resolves technical, computer, and customer service problems. Performs secondary technical review and verification of cases prior to sign-out to ensure accurate and timely billing and reporting. Education required: Bachelor’s degree in relevant field; ASCP certification preferred. EOE M/F/Disability/Vet.
Required Qualifications
- Two years of laboratory experience, required.
- Bachelor’s degree in a chemical, biological, clinical or medical laboratory science, or medical technology from an accredited institution, or Bachelor's degree equivalent education as defined in the CFR: 42CFR493.1405(b)(5)(i)(B).
- ASCP certified as MT(ASCP), MB(ASCP), or CG(ASCP) preferred
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