Senior Mechanical Engineer, Medical Devices (Hybrid)

Stryker Group; Cary (IL); Hybrid; USD 86,000 - 143,000; Full time

Job summary

Stryker Group, within the Sage business unit in Cary, IL, is seeking a Senior Engineer to lead the design and development of new medical devices across the full product lifecycle, from concept through launch. You will collaborate with R&D, QA, Manufacturing, Regulatory, and Clinical teams to ensure safe, effective designs.

The role emphasizes prototyping, testing, documenting, and adherence to design controls and quality systems, with a strong focus on translating inputs into robust

Qualifications

• BS in Mechanical, Biomedical, or related Engineering field.
• Minimum 2 years of relevant work experience.
• Ability to translate design inputs into engineering specifications and documentation.

Responsibilities

• Research, design, develop, modify, and verify mechanical components and modules for medical devices with minimal supervision.
• Translate design inputs into engineering specifications and produce subsystem-level designs.
• Prototype and analyze design solutions to validate concepts and performance.
• Apply engineering principles to solve complex technical challenges.
• Create and refine engineering documentation, including Design History Files, in compliance with design control procedures.
• Collaborate cross-functionally with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management teams.
• Understand product use and clinical procedures to inform design strategy and decisions.
• Support regulatory compliance by following industry standards, risk management, and quality system requirements.

Skills

Mechanical design

Cross-functional collaboration

Prototyping

Engineering problem solving

Education

BS in Mechanical/Biomedical Eng

Tools

Creo

GD&T

CAx/CAE tools

Job description

Stryker Group, within the Sage business unit in Cary, IL, is seeking a Senior Engineer to lead the design and development of new medical devices across the full product lifecycle, from concept through launch. You will collaborate with R&D, QA, Manufacturing, Regulatory, and Clinical teams to ensure safe, effective designs.

The role emphasizes prototyping, testing, documenting, and adherence to design controls and quality systems, with a strong focus on translating inputs into robust