Tech Surgical
Location: Naperville, IL
Profession: Tech
Posted: 8/8/2026
Salary: $0.00/weekly
Weekly Hours: 0
Shift: Mids
Job Details
Job Title
Quality Assurance Coordinator – Sterile Processing
Location
Naperville, IL
Schedule / Job Type
Contract | Full-Time | Onsite | Evening Shift (3:00 PM – 11:30 PM)
Key Responsibilities
- Monitor Sterile Processing Department (SPD) workflow, quality, and daily operations to ensure compliance with established standards.
- Perform daily process and quality tray audits, documenting results accurately within the instrument tracking system for full traceability.
- Monitor staff competencies and provide training, coaching, and re-education as needed; train new hires and assist with annual competency assessments.
- Maintain accurate quality and event reporting, including internal and external quality events (ERA reporting).
- Monitor routine equipment maintenance, troubleshoot minor equipment issues, and ensure adherence to SPD policies, manufacturer IFUs, and load-failure procedures.
- Support process improvement initiatives, attend quality meetings, and submit detailed daily reports to site management and quality/education leadership.
Required Qualifications
- Minimum of 3 years of experience as a Sterile Processing Technician.
- At least 2 years of experience in quality assurance, staff education, or supervisory responsibilities within an SPD setting.
- Active certification as a Sterile Processing Technician — CRCST or CBSPDT required.
- Demonstrated expert-level knowledge of AAMI standards, Joint Commission requirements, and Infection Prevention guidelines.
- At least 1 successfully completed travel contract in sterile processing.
- Proficiency with Epic and instrument tracking systems.
Preferred Experience / Skills
- Experience in a supervisory or lead sterile processing role with direct staff oversight responsibilities.
- Familiarity with implementing process improvements to enhance patient safety and operational efficiency.
- Strong written and verbal communication skills with experience submitting formal quality reports.
Why Join Us
- Take on a high-impact quality assurance role within a structured sterile processing environment that values compliance, patient safety, and continuous improvement.
- No floating, weekend, on-call, or holiday requirements — offering a consistent and predictable schedule.
Apply Now
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