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Test Technician I

Maple Grove, Minnesota, United States

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.

We are seeking a Test Technician I to support product engineering through a variety of testing activities that ensure our products meet regulated quality standards throughout the product development process and lifecycle. This individual will provide hands-on technical support, monitor and assemble test setups, and help identify and resolve complex issues within a collaborative, fast-paced development environment.

The ideal candidate will be highly organized and capable of setting priorities while contributing to laboratory planning and execution. This role is accountable for producing accurate, high-quality test data while maintaining strong laboratory and documentation practices to ensure regulatory compliance.

At Anteris Technologies, you’ll join a mission-driven team dedicated to improving the lives of patients with aortic stenosis through breakthrough structural heart technologies — and help build the organizational foundation supporting that impact.

 

Primary Duties and Responsibilities

  • Perform technical testing related to product functionality, including concept feasibility, design verification, and sustainment engineering, with a focus on new product development.
  • Participate in the development and review of test methods and Standard Operating Procedures (SOPs).
  • Support project teams in planning and executing test activities, including occasional coordination or oversight of colleagues or contractors.
  • Generate high-quality test data and interpret results, presenting findings to project teams.
  • Report experimental results, including unexpected findings, and support investigation of related nonconformances.
  • Support equipment validation, preventive maintenance, and repair activities as needed.
  • Liaise with third-party suppliers and external partners when required.
  • Assist with onboarding and training of other technicians as needed.
  • Maintain accurate laboratory documentation and support audit readiness.
  • Contribute positively to a collaborative, inclusive team environment that spans global locations.

 

Skills, Knowledge, Experience & Qualifications

Required Qualifications:

  • Associate’s degree, or demonstrated technical aptitude through education, hands-on experience, or relevant training.
  • Minimum of 1 year of laboratory experience in medical devices, diagnostics, or a related technical field.
  • Understanding of test protocols and technical documentation.
  • Knowledge of testing methodologies for medical device functionality.
  • Familiarity with data analysis tools and basic statistical analysis.
  • Structured, methodical approach to problem solving.
  • Understanding of industry standards and regulatory requirements for medical device testing.
  • Working knowledge of Quality Management Systems (QMS).
  • Strong communication skills with the ability to present information to both technical and non-technical audiences.
  • Ability to manage multiple priorities across concurrent projects.
  • Strong attention to detail and data management practices.
  • Ability to work with integrity in a diverse, global team environment across multiple time zones.

 

Preferred Qualifications:

  • Experience with BDC Laboratories, MTS, or Keyence test equipment.
  • Experience with Grand Avenue QMS.
  • Familiarity with SolidWorks.
  • Experience with Formlabs or Stratasys 3D printing.
  • Experience with Epilog laser cutting equipment.
  • Knowledge of ISO 5840-1, -2, and -3 standards.
  • Experience with equipment calibration.
  • Ability to interpret engineering drawings.

 

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

This is the national market pay scale.

Salary Range

$32 - $37 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.

 

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