Quality Assurance Specialist
University Hospitals · Greater Cleveland
FULL-TIME
Posted Nov 12, 2026
Job Description
Joining Our Team Comes With Several Benefits, Including
Competitive hourly rate
Free parking
Tuition reimbursement
A Brief Overview
Provides departmental management interface and quality assurance expertise to ensure departmental compliance with regulatory and accreditation agencies. Supports quality assurance activities for both the Cellular Therapy and Heme Malignancy Programs within the Seidman Cancer Center. Implements and facilitates quality goals based on the clincial and laboratory program Quality Plans.
What You Will Do
Quality review of medical and lab records associated with cellular therapy procedures and treatments.
Assists with writing, revising, and maintenance of standard operating procedures and associated forms and worksheets; facilitates reviews and approvals; ensures protocol compliance
NMDP Executes internal audits, coordinate and prepares for external audits including FACT, FDA, Joint Commission, ODH and commercial partners who provide therapeutic products to the program.
Collaborates with interdepartmental staff on quality improvement projects. Reviews and facilitates incident/accident/errors. Corrective action/follow up
Ensures programmatic compliance including but not limited to FDA, FACT (Foundation for the Accreditation of Cellular Therapy), NMDP, CIBMTR, ODH, JC.
Additional Responsibilities
Performs other duties as assigned.
Complies with all policies and standards.
For specific duties and responsibilities, refer to documentation provided by the department during orientation.
Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients. Annual training, the UH Code of Conduct and UH policies and procedures are in place to address appropriate use of PHI in the workplace.
Primary Location
United States-Ohio-Cleveland
Work Locations
11100 Euclid Avenue
Organization
Seidman_Cancer_Center_UHC
Schedule
Full-time
Employee Status
Regular
Job Type
Standard
Job Level
Professional
Travel
No
Remote Work
Hybrid
Job Posting
Nov 12, 2026, 1:21:41 PM
Education
Bachelor's Degree in science, healthcare, quality, or related discipline (Required)
Work Experience
2+ years professional experience in a healthcare related field, laboratory or experience in quality assurance (Required) and
Prior experience with process/performance improvement (Preferred)
Knowledge, Skills, & Abilities
Excellent organizational & communication skills. (Required proficiency)
Detailed oriented and be able to multi-task and handle a large volume of work. (Required proficiency)
Must possess high degree of computer skills, complex math skills, proficiency in Microsoft (Required proficiency)
Good written and verbal communication skills. (Required proficiency)
Knowledge of cellular therapy, FDA, GMP, and GTP regulations. (Required proficiency)
Office and outlook, PowerPoint, excel, and working with data bases. (Required proficiency)
Excellent oral and written communication skills (Required proficiency)
Excellent customer service orientation. (Required proficiency)
Demonstrated ability to manage processes and/or activities of various and diverse employee groups, interacting effectively and professionally. (Required proficiency)
Licenses and Certifications
Medical Technologist (MT-ASCP) (Preferred)
Healthcare Quality/CPHQ (Preferred)
Physical Demands
Standing Occasionally
Walking Occasionally
Sitting Constantly
Lifting Rarely 20 lbs
Carrying Rarely 20 lbs
Pushing Rarely 20 lbs
Pulling Rarely 20 lbs
Climbing Rarely 20 lbs
Balancing Rarely
Stooping Rarely
Kneeling Rarely
Crouching Rarely
Crawling Rarely
Reaching Rarely
Handling Occasionally
Grasping Occasionally
Feeling Rarely
Talking Constantly
Hearing Constantly
Repetitive Motions Frequently
Eye/Hand/Foot Coordination Frequently
Travel Requirements
10%
Competitive hourly rate
Free parking
Tuition reimbursement
A Brief Overview
Provides departmental management interface and quality assurance expertise to ensure departmental compliance with regulatory and accreditation agencies. Supports quality assurance activities for both the Cellular Therapy and Heme Malignancy Programs within the Seidman Cancer Center. Implements and facilitates quality goals based on the clincial and laboratory program Quality Plans.
What You Will Do
Quality review of medical and lab records associated with cellular therapy procedures and treatments.
Assists with writing, revising, and maintenance of standard operating procedures and associated forms and worksheets; facilitates reviews and approvals; ensures protocol compliance
NMDP Executes internal audits, coordinate and prepares for external audits including FACT, FDA, Joint Commission, ODH and commercial partners who provide therapeutic products to the program.
Collaborates with interdepartmental staff on quality improvement projects. Reviews and facilitates incident/accident/errors. Corrective action/follow up
Ensures programmatic compliance including but not limited to FDA, FACT (Foundation for the Accreditation of Cellular Therapy), NMDP, CIBMTR, ODH, JC.
Additional Responsibilities
Performs other duties as assigned.
Complies with all policies and standards.
For specific duties and responsibilities, refer to documentation provided by the department during orientation.
Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients. Annual training, the UH Code of Conduct and UH policies and procedures are in place to address appropriate use of PHI in the workplace.
Primary Location
United States-Ohio-Cleveland
Work Locations
11100 Euclid Avenue
Organization
Seidman_Cancer_Center_UHC
Schedule
Full-time
Employee Status
Regular
Job Type
Standard
Job Level
Professional
Travel
No
Remote Work
Hybrid
Job Posting
Nov 12, 2026, 1:21:41 PM
Education
Bachelor's Degree in science, healthcare, quality, or related discipline (Required)
Work Experience
2+ years professional experience in a healthcare related field, laboratory or experience in quality assurance (Required) and
Prior experience with process/performance improvement (Preferred)
Knowledge, Skills, & Abilities
Excellent organizational & communication skills. (Required proficiency)
Detailed oriented and be able to multi-task and handle a large volume of work. (Required proficiency)
Must possess high degree of computer skills, complex math skills, proficiency in Microsoft (Required proficiency)
Good written and verbal communication skills. (Required proficiency)
Knowledge of cellular therapy, FDA, GMP, and GTP regulations. (Required proficiency)
Office and outlook, PowerPoint, excel, and working with data bases. (Required proficiency)
Excellent oral and written communication skills (Required proficiency)
Excellent customer service orientation. (Required proficiency)
Demonstrated ability to manage processes and/or activities of various and diverse employee groups, interacting effectively and professionally. (Required proficiency)
Licenses and Certifications
Medical Technologist (MT-ASCP) (Preferred)
Healthcare Quality/CPHQ (Preferred)
Physical Demands
Standing Occasionally
Walking Occasionally
Sitting Constantly
Lifting Rarely 20 lbs
Carrying Rarely 20 lbs
Pushing Rarely 20 lbs
Pulling Rarely 20 lbs
Climbing Rarely 20 lbs
Balancing Rarely
Stooping Rarely
Kneeling Rarely
Crouching Rarely
Crawling Rarely
Reaching Rarely
Handling Occasionally
Grasping Occasionally
Feeling Rarely
Talking Constantly
Hearing Constantly
Repetitive Motions Frequently
Eye/Hand/Foot Coordination Frequently
Travel Requirements
10%
Additional Details
- City
- Greater Cleveland
- Country
- US
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