R&D Engineer II

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.

Anteris is seeking a R&D Engineer II who will be responsible for supporting the Systems design, development, and early-stage validation of innovative Class III medical devices. This role contributes to translating user needs and clinical requirements into robust product designs, collaborates cross-functionally to advance products from concept through design verification, validation, and transfer.

This is a hands-on engineering role where you will independently execute core design activities while partnering closely with Marketing, Clinical, Process Development, Quality, Regulatory, and Manufacturing to ensure designs are scalable, compliant, and aligned with customer needs and system requirements.

Main Responsibilities:

Design & Product Development:

Contribute to the design and development of a system of heart valve and catheter-based delivery tools and associated components

Generate design concepts, prototypes, and engineering solutions aligned to product requirements

Support development builds, feasibility testing, and iterative design improvements

Translate clinical, user, and system requirements into engineering specifications

Testing & Design Verification

Design and execute bench testing, characterization, and verification activities

Support the development of test methods and fixtures for device evaluation

Analyze data to evaluate performance, identify failure modes, and guide design decisions

Document results in technical reports and contribute to design history files

Cross-Functional Collaboration

Work with Marketing and Clinical to capture and translate customer needs into system requirements

Partner with valve and delivery tool design teams to ensure robust systems are delivered

Partner with Process Development to ensure system designs are manufacturable and scalable

Collaborate with Quality to support risk management, testing strategies, and documentation

Collaborate with Regulatory to ensure all standards are met and system is submission ready

Work with Manufacturing and Supply Chain to support design transfer activities

Risk Management & Documentation

Contribute to risk analysis activities (FMEA)

Support design controls in accordance with FDA and ISO standards

Participate in design reviews and ensure proper documentation within DHF

Continuous Improvement & Problem Solving:

Investigate technical challenges using structured problem-solving methods

Support root cause analysis and corrective actions during deployment

Identify opportunities to improve product performance, reliability, and usability

Skills, Knowledge, Experience & Qualifications

Required Qualifications:

Bachelor’s degree in Engineering (Mechanical, Biomedical, or related)

2-5 years of experience in medical device R&D or product development

Experience working in a regulated environment (Class III preferred)

Preferred Qualifications:

Familiarity with structural heart therapies (TAVR, TMVR highly desirable)

Experience with design controls, verification/validation, and risk management

Proficiency with CAD and prototyping tools

Experience developing test methods and analyzing engineering data

Compensation:

Target base salary range: $95,000 – $115,000, plus eligibility for an annual short-term incentive (STI) targeted at 7% of base salary and equity participation. Final compensation will be determined based on experience and alignment with role requirements. Unfortunately, we are unable to sponsor work visas (OPT, H1B, etc.) at this time.

What We Offer:

Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies.

Collaborative and dynamic work environment with a culture of innovation and excellence.

Competitive compensation package, including salary, performance-based bonuses, and stock options.

Career development opportunities and a chance to be part of a growing company that values its employees.

Health and Wellness Offerings:

Medical, Dental, and Vision Plans

Flexible Spending Account (FSA)

401k + Company Match

Life, AD&D, Short Term and Long-Term Disability Insurance

Bonus Plan Eligibility

Employee Equity Program

Paid Holidays & Vacation

Employee Assistance Program

Inclusive Team Environment

This is the national market pay scale.

Salary Range $95,000 — $115,000 USD

Note: We may require proof of COVID-19 vaccination to comply with health institutions, state, local municipality, and/or travel regulations.

Anteris Technologies recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. We have a clear vision: to be a place of belonging for all humans by promoting diversity, multiculturism and inclusion, as a goal and reflection across the organization. Diversity is more than a commitment - it is part of our mission to deliver the best structural heart products on a global scale.