QA/QC Specialist

QA/QCSpecialist-IGMClinicalAdmin

Columbus, Ohio, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“QA/QC Specialist - IGM Clinical Admin at QA/QC Specialist. Skills: Quality control, Operational improvement, Compliance, Inspection readiness. Promote compliance with regulatory requirements. Assist with inspections and inspection readiness”

What You'll Achieve.

Ensure accurate and timely billing and reporting

Industry & Context.

Problems you'll solve

Troubleshooting; Problem-solving; Solves problems regarding deviations; Resolves technical, computer, and customer service problems

Eligibility Requirements

Biohazard waste, Blood and/or Bodily Fluids, Chemicals/Medications, Climb stairs/ladder, Communicable Diseases and/or Pathogens, Decision Making, Fume /Gases /Vapors, Lifting / Carrying: 11-20 lbs, Lifting / Carrying: 21-40 lbs, Loud Noises, Pushing / Pulling: 0-25 lbs, Pushing / Pulling: 26-40 lbs, Pushing / Pulling: 41-60 lbs, Reaching above shoulder, Bend/twist, Squat/kneel, Audible speech, Color vision, Computer skills, Depth perception, Flexing/extending of neck, Hand use: grasping, gripping, turning, Hearing acuity, Interpreting Data, Lifting / Carrying: 0-10 lbs, Peripheral vision, Problem solving, Repetitive hand/arm use, Seeing – Far/near, Sitting, Standing, Walking

What They're Looking For.

Must Have

Two years of laboratory experience

Nice to Have

American Society for Clinical Pathology (ASCP) certified as an MT(ASCP), MB(ASCP), or CG(ASCP), Experience in cytogenetics, molecular genetics, or molecular biology

What You'll Do.

Promote compliance with regulatory requirements

Assist with inspections and inspection readiness

Lead group training for education

Coordinate the IGM Quality Monitoring program

investigate incidents

Track and review laboratory documentation

Facilitate the creation

and distribution of SOPs

Collaborate to coordinate process improvements

Implement new workflows

Facilitate and lead workgroups and projects

Perform in-depth troubleshooting

Solve problems regarding deviations

and customer service problems

Perform secondary technical review and verification

How You'll Work.

Team & Collaboration

Collaborates with supervisor and manager; Foster interpersonal relationships with internal and external customers

Communication Scope

Excellent communication skills; Effectively decipher and present information through oral and written communication

Process & Methodology

Facilitates and leads workgroups and projects

Full Job Description

**Overview:** **Job Description Summary:** Coordinates quality control, operational improvement, compliance and inspection readiness, and education within the Institute for Genomic Medicine. Assists with troubleshooting and provides technical guidance. **Job Description:** **Essential Functions:** * Promotes compliance with the regulatory requirements of the laboratory, raising awareness of CAP/CLIA, Joint Commission, and NYS Testing requirements. Serves as General Supervisor as defined by CAP/CLIA guidelines and Lab Supervisor as defined by New York State testing guidelines as applicable. * Assists with inspections and inspection readiness throughout the year. 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 Requirement:** 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 Code of Federal Regulations: 42CFR493.1405

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