Senior Process Development Engineer

Anteris Technologies•Maple Grove, MN

12h•$118,000 - $138,000•Onsite

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 Senior Process Development Engineer to lead the development, validation, and commercialization readiness of manufacturing processes supporting our transcatheter heart valve system and associated delivery components. This role is responsible for translating design intent into robust, scalable, and compliant manufacturing processes suitable for pivotal clinical and commercial production. The position partners closely with R&D, Quality, Regulatory, Supply Chain, and Manufacturing to ensure process capability, documentation integrity, and regulatory readiness. This is a hands-on, technically deep role with strategic impact as we scale toward commercialization. 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.

Requirements

Bachelor’s degree in Mechanical, Biomedical, Industrial, or related Engineering discipline with 5+ years of experience in Process Development or Manufacturing Engineering within Class III medical devices. 3+ years’ experience with a graduate degree.
Demonstrated experience executing IQ/OQ/PQ/PPQ and Test/ Inspection Method Validation in a regulated environment.
Experience with design transfer from development into regulated production.
Strong knowledge of FDA 21 CFR Part 820, ISO 13485, and EU MDR expectations.
Hands-on experience with fixture design, process automation, and equipment qualification.
Proven ability to lead cross-functional initiatives and influence without direct authority.
Proficient in technical documentation and verbal communication.
Ability to use microscopes and other magnification equipment

Nice To Haves

Degrees in Engineering or Chemical Engineering and/or an advanced degree (MS) in Engineering or related field desired.
Direct experience with catheter-based or structural heart devices strongly preferred.
Experience with transcatheter heart valves (TAVR, TMVR, TPV) or delivery systems.
Experience working in a pre-commercial or scaling organization.
Background in Class III medical devices
Knowledge of ISO 5840-1/ -3.

Responsibilities

Plan and execute development and optimization of manufacturing processes for Class III transcatheter heart valves.
Drive process characterization, improvements, and capability studies to establish robust and commercial-ready valve manufacturing processes.
Provide DFM/DFA input during product development to ensure manufacturability and cost efficiency.
Support global manufacturing alignment as processes are standardized and scaled.
Author and execute validation strategies, including IQ, OQ, PQ/PPQ, TMV, IMV and equipment qualifications in alignment with the Master Validation Plan and applicable regulatory requirements (FDA, ISO 13485, and EU MDR).
Ensure robustness of the validation packages meeting industry requirements for auditability and regulatory compliance. are audit-ready and inspection-ready.
Partner with R&D, Quality and Regulatory during process developments, regulatory submissions and periodic inspections.
Support risk management activities including PFMEA and control plan development.
Evaluate and implement emerging technologies for semi-automated and automated solutions for fixture design, assembly processes, and test methods, including establishing equipment specification, and vendor selection.
Improve repeatability and reduce operator variability through fixture optimization and automation strategies.
Evaluate and implement bioburden solutions for valve manufacturing, ensuring effectiveness and process compatibility.
Improve and establish visual inspection methods for tissue and valve manufacturing, ensuring repeatability and reproducibility.
Plan and execute product performance and functional assessments associated with process changes and improvements.
Drive design transfer activities from R&D to Manufacturing.
Develop manufacturing documentation including SOPs, work instructions, process flows, and training materials.
Provide on-floor technical support for complex builds, process deviations, and yield improvements.
Investigate nonconformances and drive root cause analysis and CAPA execution.
Identify opportunities to improve yield, reduce scraps, and enhance cycle time.
Lead structured problem-solving initiatives using data-driven methodologies.
Support cost-of-goods reduction initiatives while maintaining compliance and product performance.
Follow the Anteris Quality Management System and comply with all applicable procedures and training requirements.