Mechanical Engineer II

Agiliti•Milwaukee, WI

25d

About The Position

Agiliti is a provider of medical equipment management and service solutions. The Mechanical Engineer II helps develop innovative medical products from concept through production, working with engineering, quality, regulatory, certification, clinical verification, manufacturing, and business teams. The role leads complex engineering projects and contributes to system integration, product design, prototyping, testing, troubleshooting, production readiness, and continuous improvement. The engineer uses 3D design and analysis tools, prototyping technologies, and equipment such as SolidWorks, 3D printers, and CNC equipment. The role supports product risk analysis, usability, verification, certification testing, design transfer, and initial production. It also investigates field failures, identifies root causes, develops corrective actions, applies risk-based design practices, leads design reviews, and helps identify new technologies and intellectual property. The position may require travel up to 25% domestically and internationally. Agiliti may require certain vaccinations or proof of vaccination status based on customer or company requirements; if required, the company provides directions and covers the expense at a participating clinic.

Requirements

Bachelor of Science in Mechanical Engineering, Biomedical Engineering, or a related field.
3–5 years of experience designing products in the medical, consumer, automotive, or aerospace industry.
Understanding of mass-production manufacturing processes, including injection molding, blow molding, welded steel structures, sheet metal stamping and forming, die casting, and CNC technologies.
Experience with 3D design and analysis tools and prototype production technology.
Versatility in entrepreneurial organizations, demonstrated through increasing responsibilities and willingness to scale abilities to complete objectives.
Experience creating and leading collaborative teams through complex projects.
Experience in DFM, DFA, DFMEA, or other risk-based design strategies.
Experience designing for agency certifications such as ISO, IEC, AAMI, UL, CE, CISPR, FCC, or FDA.
Experience working with project management software and Scrum-type environments.
Demonstrated financial acumen.
Strong interpersonal communication and presentation skills.
Experience in healthcare product development or a similarly federally regulated field.
Exceptional SolidWorks 3D CAD skills, including robust parametric models and top-down, master-model-driven assemblies.
Analytical thinking and ability to develop effective solutions to technical problems.
Ability to apply relevant industry and process standards to work.
Strategic perspective and ability to keep overall objectives in mind.
Ability to manage client needs and relations effectively.

Nice To Haves

Familiarity with other technical disciplines such as electrical engineering and embedded firmware.
Prior experience with the 60601 family or other FDA-related standards is a significant plus.
Prior experience interfacing with certification bodies such as Intertek, UL, or TUV.
Experience using computational tools for structural analysis (FEA) and dynamic mechanical performance is a significant plus.

Responsibilities

Lead multiple complex engineering projects and support system integration across product development initiatives.
Design, analyze, prototype, test, and troubleshoot mechanical components and electromechanical systems.
Use SolidWorks, 3D printers, CNC equipment, and other tools to develop and evaluate prototypes.
Support product risk analysis, usability, verification, and certification testing.
Partner with Engineering, Quality/Regulatory, Certification, Clinical Verification, and business teams to develop effective solutions.
Work with manufacturing partners on design transfer, production readiness, test fixtures, and initial production samples.
Investigate field failures, identify root causes, and develop corrective actions.
Apply DFM, DFA, DFMEA, and other risk-based design practices.
Lead design reviews and communicate complex technical concepts to internal teams and external partners.
Identify opportunities for new technologies, process improvements, and intellectual property.
Participate in ISO and AAMI standards development.
Keep skills and specializations up to date with industry developments.
Manage client needs and relations effectively.
Travel up to 25% domestically and internationally.