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Salary
≈ $20k – $50k per year (Estimated)
Location
In office (Heredia)
Seniority
Junior
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 21, 2026. First seen by Alion on Oct 13, 2026. Stryker scores B on the Alion truth index.

Overview
Company
Impact
Profile match
Stryker is an American medical technology company founded in 1941 by an orthopaedic surgeon who began manufacturing the mobility devices he had designed for his own patients. It sells hip and knee implants, trauma and extremity fixation, spinal implants, surgical power tools and navigation, neurovascular devices, hospital beds and stretchers, emergency response equipment, and the Mako robotic arm used for joint replacement. Listed on the New York Stock Exchange, it is one of the largest orthopaedic device makers in the world. The company is headquartered in Portage, Michigan, United States.
Work Flexibility: Hybrid

Associate Engineer, Patient Specific Solutions

Join a team focused on transforming clinical imaging and engineering data into patient-specific solutions that support surgical procedures. In this role, you will apply engineering and CAD expertise to create and review customized devices, surgical planning materials, and technical documentation within a regulated medical device environment. You will collaborate with cross-functional partners to support design, manufacturing, quality, and regulatory requirements.

What You Will Do

  • Design and modify patient-specific mechanical components and instrumentation using CAD software in accordance with approved design requirements.

  • Review clinical imaging data, including CT scans and X-rays, to support device design and surgical planning activities.

  • Create pre-operative alignment reports, surgical planning guides, and operating instructions for patient-specific solutions.

  • Develop and maintain technical drawings and 3D models that provide manufacturing and inspection teams with complete design information.

  • Perform engineering calculations and design verification activities to support product development and design validity.

  • Investigate design-related issues, conduct root cause analysis, and evaluate potential solutions against defined requirements.

  • Review and verify pre-operative reports, device designs, and specifications completed by peers to support quality standards.

  • Collaborate with Quality, Manufacturing, Regulatory Affairs, Clinical, Marketing, and Project Management teams to support project execution and compliance objectives.

What You Will Need

Required Qualifications

  • Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, or a related Engineering discipline.

  • Minimum 0 years of professional engineering experience.

  • Intermediate proficiency with CAD software such as SolidWorks, Siemens NX (Unigraphics), or similar modeling tools.

  • Intermediate English proficiency (minimum B2 level).

  • Proficiency in Microsoft Office applications.

  • Ability to read and interpret engineering drawings and technical documentation.

Preferred Qualifications

  • Knowledge of orthopedic or mechanical medical device products.

  • Knowledge of radiology concepts and applicable ASTM or ISO standards.

Travel Percentage: 0%
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