Senior Mechanical Design Engineer(Hybrid)

Stryker • Portage, MI

49d • Hybrid

About The Position

At Stryker, we share a bold mission: Together with our customers, we are driven to make healthcare better. Every day, we push boundaries to improve lives through groundbreaking medical technologies. Our Interventional Spine team leads the way in creating minimally invasive solutions that restore mobility, relieve pain, and transform patient outcomes. We're looking for a Senior Design Mechanical Engineer to join our dynamic team of innovators at our Portage, Michigan headquarters. This hybrid role requires at least three days onsite, offering the perfect blend of collaboration and flexibility. As a Senior Design Engineer, you'll partner across disciplines—Quality, Manufacturing, Regulatory, Clinical Sciences, Marketing, and Project Management—to drive success. Under minimal supervision, you'll have the chance to work on cutting-edge systems and play a pivotal role in designing and delivering next-generation spine devices that truly make a difference. Learn more about our business here: Stryker IVS What you will do Design & Development: Research, design, develop, and verify medical device components and sub-systems with minimal supervision. Specifications & Solutions: Translate design inputs into engineering specifications; develop and prototype solutions to validate concepts. Problem Solving: Apply fundamental and advanced engineering principles to analyze and resolve complex issues. Customer & Clinical Insight: Demonstrate a strong understanding of customer needs, product use, and clinical procedures. Compliance & Documentation: Adhere to industry standards and regulatory requirements; create and refine engineering documentation, including Design History Files. Quality & Risk Management: Follow design controls and risk management processes per the Quality Management System. Cross-Functional Collaboration: Work closely with R D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management to ensure project success. Ownership & Leadership: Prioritize work independently, contribute to complex projects, and build strong team relationships.

Requirements

• Bachelor of Science in Engineering, Mechanical Engineering, BioMedical, or related discipline.
• 2+ years of relevant work experience.
• Working knowledge and understanding of mechanical engineering practices and design principles.

Nice To Haves

• Experience working in the medical device industry.
• Knowledge of design and concept generation CAD or CAE modeling tools (Creo preferred)
• Knowledge of analysis tools (i.e., DFMECA, Fault Tree Analysis, FEA, Stack-ups, etc.) and statistical methods (i.e., leveraging Minitab for ANOVA, normality testing, confidence calculations, etc.).
• Technical ability to create engineering drawings and models, applying GD&T and CAE tools.
• Demonstrated ability to apply knowledge of materials and manufacturing processes to product design.

Responsibilities

• Research, design, develop, and verify medical device components and sub-systems with minimal supervision.
• Translate design inputs into engineering specifications; develop and prototype solutions to validate concepts.
• Apply fundamental and advanced engineering principles to analyze and resolve complex issues.
• Demonstrate a strong understanding of customer needs, product use, and clinical procedures.
• Adhere to industry standards and regulatory requirements; create and refine engineering documentation, including Design History Files.
• Follow design controls and risk management processes per the Quality Management System.
• Work closely with R D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management to ensure project success.
• Prioritize work independently, contribute to complex projects, and build strong team relationships.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees