Quality Assurance / Quality Engineering Opportunities
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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. Quality is foundational to everything we do at Anteris Technologies. As we continue advancing next-generation structural heart therapies, we are building a strong pipeline of quality professionals who are passionate about compliance, continuous improvement, and protecting patient safety. We are interested in connecting with candidates who have experience in quality engineering, quality systems, document control, microbiology, inspection, validation, CAPA, nonconformance management, auditing, sterilization support, or regulatory compliance within regulated industries. Ideal candidates have experience working within FDA and/or ISO-regulated environments and possess strong analytical skills, attention to detail, and a collaborative mindset. Experience supporting Class II or Class III medical devices, biologics, cleanroom operations, or manufacturing quality systems is highly valued. Join a mission-driven organization where quality plays a direct role in delivering life-changing technologies to patients around the world. Compensation for roles within this talent community varies based on specialization, technical expertise, and level. Typical salary ranges may include: Quality Systems / Documentation roles: $65,000 - $75,000 Microbiology roles: $60,000 - $90,000 Quality Engineering and specialized scientific roles: Engineer II: $85,000 - $110,000 Senior Engineer: $115,000 - $140,000 Principal Engineer: $140,000 - $160,000 Eligible positions may also participate in annual incentive and equity programs.
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