Manufacturing Engineering Technician, Sr.

Anteris Technologies•Maple Grove, MN

4h•$36 - $44

About The Position

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 Sr Manufacturing Engineering Technician to provide hands-on technical support to the manufacturing engineering team. This role focuses on equipment setup and maintenance, fixture and tooling development, routine testing, data collection, and technical documentation. Working under the guidance of senior staff, the individual will help ensure efficient day-to-day operations while supporting manufacturing processes, process development, and continuous improvement efforts. 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.

Requirements

Associate’s degree in a technical field, trade school certification, or equivalent hands-on experience with 5-10 years of experience in a regulated manufacturing or engineering environment (medical device, pharma, aerospace, or similar).
Strong knowledge of equipment operating principles, and measurement tools (calipers, micrometers, gauges).
Comfort working in controlled environments (e.g., cleanrooms) when required.
Proficiency with computer skills for data entry and, documentation (Excel, Word, Outlook, and PowerPoint)
Strong attention to detail, willingness to learn, and ability to follow procedures.
Effective verbal and written communication skills.
Experience with equipment calibration, preventive maintenance, or testing processes.

Nice To Haves

Proficiency with CADs (SolidWorks, Corel Draw, etc) and engineering drawings.
Experience working with 3D printers, laser cutting,
Prior experience in a regulated environment (ISO 13485, FDA, or similar).
Experience in tissue heart valve manufacturing, including tissue processing, solution preparation and sewing.

Responsibilities

Perform assigned tasks in compliance with company procedures, safety requirements, and the Quality Management System.
Manage and execute preventive management (PM) activities for manufacturing equipment and support routine PM efforts as needed.
Assist engineers with equipment setup, qualification activities (IQ, OQ, PQ), and validation of test and inspection methods.
Support the design, development, and fabrication, and prototyping of manufacturing aids, tooling, and fixtures.
Assist with testing activities, sample preparation, data collection, and documentation of results.
Develop, maintain, and organize manufacturing training materials, and support the onboarding and training of new hires (e.g., production assemblers or operators).
Operate laboratory and test equipment as trained; perform basic troubleshooting and escalate equipment issues, nonconformances, or deviations in accordance with quality procedures.
Identify procedural gaps and recommend revisions, corrections, or process improvements to enhance clarity, compliance, and efficiency.
Follow GDP and accurately record results and maintain records using established formats and systems.
Perform basic cleanroom support activities (e.g., material handling, environmental monitoring) as required.
Follow gowning procedures and maintain compliance with controlled environment standards (e.g., ISO Class 7/8 cleanroom standards).
Participate in training, continuous improvement initiatives, and cross-functional activities as assigned.
Carry out other duties as assigned by the manager or delegate.