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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. The  Manufacturing Technician   is responsible for  performing precision assembly, processing, and inspection of Class  II &  III medical devices in a highly regulated environment. This role ensures products are manufactured  in accordance with  approved procedures, quality standards, and regulatory requirements, contributing directly to the delivery of safe and effective medical devices.   Production & Assembly   Perform assembly, processing, and packaging of medical devices following detailed work instructions and SOPs   Execute tasks requiring precision, attention to detail, and fine motor skills   Operate manufacturing equipment and tools  in accordance with  established procedures   Meet production targets while  maintaining  strict quality standards   Quality & Compliance   Follow FDA regulations, ISO 13485 standards, and Good Manufacturing Practices (GMP)   Complete  accurate  documentation  in accordance with  Good Documentation Practices (GDP)   Perform in-process inspections and  identify  nonconformances   Escalate quality or safety concerns to leadership as appropriate   Team & Operational Support   Collaborate with team members and cross-functional partners to support production goals   Participate in training, cross-training, and continuous learning initiatives   Maintain a clean, organized, and compliant work environment   Support process improvements and lean manufacturing activities   Process Development & Optimization   Support process transfer from development through validation and commercialization for Class II & III medical devices   Support development, characterization, and optimization of balloon catheter and steerable sheath manufacturing processes including braiding, reflow, thermal bonding, adhesive bonding, and handle assembly operations   Drive manufacturing improvements focused on efficiency, reliability, and reduction of manual variability   Support root cause investigations, and continuous improvement initiatives   Apply problem-solving methodologies to resolve technical issues   Participate in risk management activities  in accordance with  ISO 14971 and FDA quality system requirements   Validation & Compliance   Contribute to validation activities including IQ, OQ, PQ, TMV, and IMV   Support engineering in development of protocols, reports, and technical documentation  in accordance with  GMP and regulatory requirements   Create and  maintain  work instructions and related engineering documentation   Support equipment qualification, calibration activities, and test met