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Anteris® Technologies is a global structural heart company dedicated to revolutionizing cardiac care. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team. Our mission is to forge new frontiers in cardiac care by pioneering science-driven and measurable advancements to restore heart valve patients to healthy function. Transcatheter Aortic Valve Replacement (TAVR) technologies were originally designed for older, high-risk patients. Today, younger, more active patients need a better solution that will not just open and close but restore healthy heart function. We seek to restore healthy blood flow patterns by creating the world’s first biomimetic TAVR valve, DurAVR® THV. This cutting-edge valve, incorporating our proprietary ADAPT® anti-calcification technology, is designed to mimic the natural function of a healthy heart valve. Reporting to the Director of Quality, the Disinfection & Quality Control (QC) Assistant supports the manufacture of medical devices by performing quality and material control activities such as disinfection of reusable items, material release inspection, dispatch of test samples, receipt and dispatch of garments and mops, inspection of packaged product, environmental monitoring plus cleaning of material for production staging.  This is a highly visible and supportive role, making a positive contribution to our organization’s success! At Anteris® Technologies, you'll be part of a team dedicated to enhancing the quality of life for patients with aortic stenosis through groundbreaking medical devices. Join us in our mission to revolutionize structural heart solutions.   Key Responsibilities: Quality Control            Disinfection of reusable material using washer disinfectors Executing autoclave cycles & autoclave maintenance (vacuum leak test, B&D testing). Release of reusable material post-autoclave and disinfection. Perform release of material using starting material specifications (SMS’s). Receipt of incoming tissue deliveries for use in the manufacture of a biological medical device. Inspection of packaged product using acceptance quality level (AQL) procedures. Perform environmental monitoring (EM) in a clean room setting and execute associated microbiological plate reading. Monitoring and cleaning of equipment (refrigerators, freezers). Attend departmental and organisational meetings as required. Material Handling        Accurately pick and pass-through materials for production according to stock requests. Label released material and store appropriately. Assist with packing product shipments according to work orders. Receipt and dispatch of garments and mops. Operate walkie-stacker, pallet jacks, and other material-handling equipment safely and efficiently. Back-up for the Material Coordinator as required. Inventory Management            Assist with the conduct regular cycle counts and physical inventory checks. Follow FEFO (First Expired, First Out) principles for materials with shelf lives. Ensure materials are properly stored, labelled, and organized to maintain traceability of batch/lot numbers and expiration dates. Work closely with the Quality team to ensure materials meet quality standards before use in production. Work closely with the production team to provide materials needed for manufacturing in a timely manner. Transfer of final product between quarantine and release. Documentation and Compliance         Follow established procedures for disinfection, material release, EM, and AQL in compliance with ISO 13485 and FDA regulations. Complete all required documentation accurately, including disinfection cycle records, EM records, incoming tissue receipt forms and Starting Material Specification (SMS)