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Medical Supply Technician (Sterile Processing) - Quality Assurance
- Charleston, South Carolina, United States
- Charleston, South Carolina, United States
À propos
Qualifications
English Language Proficiency: Proficient in spoken and written English.
Citizenship: United States Citizenship; non‑citizens only if no qualifying citizens available.
Experience or Education:
• One year experience equivalent to the next lower grade level (GS‑07).
• One year above high school with at least 6 semester hours in health‑care related courses such as sterile processing, nursing assistant, or hospital corpsman.
• Equivalent combination of experience and education acceptable.
Knowledge, Skills, and Abilities:
• Knowledge of fact‑finding and investigative techniques to evaluate work processes.
• Ability to analyze data and make recommendations to correct quality control problems.
• Knowledge of sterile processing operations, infection control procedures, and Joint Commission requirements for compliance during quality assurance reviews.
• Ability to compile information, evaluate facts, document findings, and prepare reports.
• Thorough knowledge of aseptic principles and techniques to maintain quality control.
• Ability to communicate effectively with technical and professional staff regarding the proper use of delicate instruments and equipment and resolve problems.
Preferred Experience:
• Three years Sterile Processing or procedural experience.
• Progressive leadership experience.
• Certification – Sterile Processing.
• Quality assurance experience with equipment.
Duties
Demonstrate comprehensive knowledge of all SPS functions and serve as liaison to end‑user services.
Monitor SPS and end‑user areas to ensure procedures are followed and items are safe and delivered on time.
Conduct systematic reviews of completed work and process documentation to assess adherence to SOPs and evaluate quality and quantity of work produced by SPS staff.
Prepare various quality assurance reports for higher‑level supervisors.
Manage quality aspects of reprocessing activities inside and outside the SPS work area, including training and competency assessment.
Plan, develop, direct, and maintain a Quality Control Program that ensures product quality through random sampling, biological testing, and product assessment.
Ensure availability and control of reusable medical/surgical supplies and equipment.
Audit all locations where critical and semi‑critical RMD are utilized, reprocessed, and stored to ensure compliance with SPS/RMD directives and industry standards.
Coordinate with project team members to plan, develop, and monitor cost, schedule, quality, and risk mitigation strategies for instrument tracking programs.
Mentor new employees and assist with the New Employee Education Program in quality assurance and instrument tracking.
Perform other related duties as assigned.
Work Schedule 5:00 pm – 1:30 am Monday – Friday (with on‑call requirements).
Benefits and Compensation
Competitive salary with regular increases; higher step rate may be considered for extra qualifications.
Paid Time Off: 37‑50 days of annual PTO (13‑26 days leave, 13 days sick, 11 paid federal holidays).
Parental Leave: up to 12 weeks of paid leave after 12 months of employment.
Child Care Subsidy: up to 25 % of eligible childcare costs for employees with family income below $144,000.
Traditional federal pension (5 years vesting) and federal 401(k) with up to 5 % VA contribution.
Federal health/vision/dental/term life/long‑term care insurance.
Telework: Not Available; Virtual: Not a virtual position.
EEO Statement All qualified applicants will receive equal employment opportunity regardless of race, color, religion, sex, national origin, veteran status, or disability.
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Compétences linguistiques
- English
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