Engineering in Tucson

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Job DescriptionJob DescriptionDescription:

Tucson, AZ |Temporary-Full-time, Hourly | On-site

About SynCardia Systems LLC

SynCardia develops, manufactures, and commercializes the SynCardia Total Artificial Heart (STAH), the only commercially available total artificial heart approved by both the U.S. Food and Drug Administration (FDA) and Health Canada. SynCardia is a wholly owned subsidiary of Picard Medical Inc. (NYSE: PMI) which became a publicly traded company on August 29, 2025.

Why this role matters:

At SynCardia our mission is to transform and save lives through life sustaining Total Artificial Heart technology. As an R&D Engineering , you’ll directly support engineering teams developing and improving our artificial heart systems through hands-on design, prototyping, testing, data analysis, and strong documentation practices. Your contributions help keep development work aligned with performance, schedule, and cost objectives in a regulated medical device environment.

What you will do:

Under the direction of senior engineering staff, you will support research and development activities across design, build, test, and documentation workflows, including:

• Create and update 3D CAD models, detailed drawings, and bills of materials for components, fixtures, and assemblies.
• Support prototype builds and bench-top experiments, including part preparation, assembly, and coordination with internal teams and external suppliers.
• Build, assemble, and troubleshoot test fixtures and setups for mechanical, electrical, and/or biological verification activities.
• Prepare test samples; execute experiments, tests, and measurements; collect data and maintain accurate lab records.
• Analyze results (e.g., Excel) and document outcomes in technical summaries, protocols, and reports.
• Present results and recommendations; participate in design reviews and technical meetings.
• Under supervision, support design controls and quality documentation (requirements traceability, risk documentation, test plans, and change documentation).
• Assist with troubleshooting and root-cause analysis of design/manufacturing issues and propose improvements through designated channels.
• Follow safety procedures and good documentation practices; help maintain an organized lab/work area and proper equipment use.
• Develop an understanding of regulatory and quality system requirements applicable to SynCardia products as directed.
• Perform other duties as assigned.

Requirements:

What we are looking for:

Required

• Currently enrolled in a Bachelor’s or Master’s degree program in Mechanical, Biomedical, Electrical, Systems Engineering, or related field (or equivalent).
• Strong verbal and written communication skills, including technical writing and clear data presentation.
• Strong organizational skills; attention to detail; ability to prioritize and manage multiple tasks
• Collaborative team player with the ability to work independently with appropriate guidance
• Hands-on aptitude for laboratory/bench work and willingness to follow written procedures.
• Working knowledge of 3D CAD (SolidWorks ) and the ability to create/read engineering drawings.
• Basic proficiency with data analysis tools (Excel required)
• Proficient in modern work management and communication tools (e.g., Outlook, Teams, SharePoint).

Nice to have

• Coursework in engineering fundamentals relevant to the position (e.g., mechanics/materials, fluids, circuits, instrumentation, controls, statistics, etc).
• Prior academic project, laboratory, or internship experience related to design, prototyping, or testing.
• Interest in medical devices and awareness of documentation and design controls expectations.
• Experience with additional analysis/test tools (e.g. LabVIEW) and familiarity with common measurement/test equipment (e.g., calipers, gauges, multimeter, DAQ equipment) with training.

Why you will love working here:

• Mission-driven work with direct patient impact
• Hands-on engineering experience in a regulated medical device R&D environment.
• Collaborative, cross-functional teams and exposure to best practices in design, verification testing, and documentation.

Work environment:

Office-based role with minimal noise, requiring extended periods of sitting, typing, and occasional lifting to 25 pounds.

Work is performed in an office and engineering laboratory with moderate noise levels (may include limited time in manufacturing areas as assigned); occasionally requiring extended periods of sitting, typing, and occasional lifting to 25 pounds, work near moving mechanical parts; work around fumes, airborne particles, or toxic chemicals; exposure to extreme heat or cold (non-weather). May require the use of appropriate personal protective equipment (PPE) when working in laboratory or manufacturing areas.

Industry:

Medical equipment manufacturing

Employment type:

Temporary-Full-time, Hourly

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