Mechanical Engineer II

Who We Are Agiliti is a leading provider of medical equipment management and service solutions, helping healthcare organizations improve patient outcomes and keep critical equipment ready for use. As a Mechanical Engineer II, you’ll help develop innovative medical products from concept through production while collaborating with engineering, quality, regulatory, certification, and manufacturing teams.

What's in it for You?

Lead meaningful engineering projects from concept through implementation.

Work hands-on with product design, prototyping, testing, and manufacturing.

Collaborate with cross-functional teams to solve complex technical challenges.

Help develop innovative medical products that support better patient care.

Build expertise in regulated product development, certification, and advanced manufacturing technologies.

What You Will Do in This Role?

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 Solid Works, 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 clearly 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.

What You Will Need for This Role?

Bachelor of Science in Mechanical Engineering, Biomedical Engineering, or related field required.
3 - 5 years of experience designing products in the medical, consumer, automotive, or aerospace industry.

Understanding of and familiarity with mass production manufacturing processes for consumer products, 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.

Proven versatility in both large and small entrepreneurial organizations as demonstrated by succession in responsibilities and willingness to scale abilities to complete objectives.

Experience in creating and leading collaborative teams through complex projects.

Familiarity with other technical disciplines such as EE and embedded firmware preferred.

Experience in DFM, DFA, DFMEA, or other risk-based design strategies.

Experience designing for agency certifications (e.g., ISO, IEC, AAMI, UL, CE, CISPR, FCC, FDA) required. Prior experience with the 60601 family or other FDA related standards is a significant plus.

Prior experience interfacing with Certification bodies (Intertek, UL, TUV) preferred.

Prior experience working with project management software and Scrum type environments (Jira, Monday, Todoist, etc.).Demonstrated financial acumen.

Strong interpersonal communication and presentation skills.

Experience in Healthcare product development or similarly Federally regulated field.

Exceptional 3D CAD skills (Solid Works) for creating robust parametric models; top-down “master model”-driven assemblies.

Experience using computational tools for structural analysis (FEA) and dynamic mechanical performance a significant plus.

Analytical Thinking – Capable of understanding a technical…