Microbiology Reprocessing Technician

Job Title Microbiology Reprocessing Technician System Job Title Technician – Microbiology Reprocessing Division/Business Unit/Line Product Service Department/Section MHS Reporting Directly Reports To: Biological Team Lead Functionally Reports To: Biological Team Lead Position Summary The Microbiology Reprocessing Technician is responsible for executing laboratory-based studies related to reusable medical device validation, including cleaning validation, disinfection efficacy, drying time, and lifecycle (simulated use) testing. This role focuses on hands‑on laboratory execution in accordance with applicable standards such as ISO 17664, AAMI TIR12/TIR30, ISO 15883, ISO 11737, and GLP/ISO 17025 requirements. The technician supports study setup, execution, and documentation in a fast‑paced, regulated environment. Key Responsibilities Execute reprocessing validation studies: cleaning validation (manual and automated), disinfection efficacy studies, dry time and residual moisture assessments, simulated use/lifecycle testing of reusable devices. Perform test article preparation, including soiling, inoculation, and device assembly/disassembly. Operate and maintain washer‑disinfectors, sterilizers, drying equipment, and related test systems. Follow and execute approved protocols, SOPs, and work instructions. Accurately document all study activities, observations, and results in accordance with GLP and ISO 17025 requirements. Support equipment qualification, calibration, and validation activities. Identify and communicate deviations, unexpected results, or issues to Study Directors or management. Maintain laboratory organization, cleanliness, and compliance with safety and quality standards. Collaborate with cross‑functional teams to support study timelines and deliverables. Contribute to continuous improvement initiatives related to workflow, efficiency, and quality. Other duties as assigned. Additional Responsibilities Support the company’s vision and mission statement. Adhere to all company policies and procedures as outlined in the corporate policies and the employee handbook. All employees are responsible for general cooperation and support of all company locations. Education and Experience Minimum of high school diploma. 0–3 years of laboratory experience (medical device, pharmaceutical, or microbiology preferred). Experience with aseptic technique and laboratory best practices. Experience in regulated environments (GLP, ISO 17025) preferred. Technical / Business Unit Related Skills & Knowledge Hands‑on experience with laboratory testing and sample handling. Ability to follow detailed procedures and protocols with high accuracy. Strong attention to detail and organizational skills. Ability to manage multiple tasks in a fast‑paced environment. Basic understanding of microbiology and contamination control principles. Strong communication and teamwork skills. Ability to work independently with guidance. Proficiency with Microsoft Office tools. Work Area Medical Devices & Healthcare. Location Country/Region: United States. Job Location: New Brighton (Onsite). Employment Information Working Model: Onsite. Employment Type: Full time / regular. Company: TÜV SÜD America Inc. Org Unit Code: MICR‑BIO. Requisition ID: 4696. #J-18808-Ljbffr