Are you a strategic systems thinker ready to lead innovation in medical technology?Â
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At Stryker, we’re seeking a Principal Systems Engineer in R&D to drive complex system design and influence the future of healthcare solutions. Join a collaborative team where your leadership and technical expertise will shape products that improve lives globally.Â
To learn more about Stryker’s Sage portfolio click here: Sage
You will need to live within commuting distance of our Cary, Illinois office. This is a hybrid role, with on-site work required Monday through Wednesday and the flexibility to work remotely the remainder of the week.
What You Will DoÂ
Lead the design, development, and integration of complex medical device systems across disciplinesÂ
Translate user needs into system requirements and guide architectural developmentÂ
Direct system integration and verification efforts, ensuring compliance and performanceÂ
Mentor engineers and influence resolution of complex design challengesÂ
Drive technology exploration, prototyping, and intellectual property developmentÂ
Collaborate with internal and external stakeholders to align technical strategies with clinical needsÂ
Lead improvements to engineering processes, tools, and cross-functional collaborationÂ
Contribute to Product Risk Management activities, including identification of failures, mitigations, safety requirements, and design for safety.
Strategize and execute customer-facing activities like voice of customer and customer centric design across the business.
Collaborate on Financial /business modeling and supports business reviews to validate a technical approach.
What You Will NeedÂ
Required QualificationsÂ
Bachelor’s degree in Software, Electrical, Mechanical, Systems, or Biomedical Engineering.
Minimum 8 years of relevant engineering experienceÂ
Proven expertise in digital system architecture, requirements decomposition, and verificationÂ
Experience applying regulatory standards such as ISO 13485 and ISO 14971Â
Proven strong communication skills for cross-functional and cross-business collaboration
Preferred QualificationsÂ
Proficiency with Requirements Management Software (e.g., Jama)Â
Experience with SysML and Model-Based Systems Engineering (MBSE)Â
Working knowledge of appropriate regulations and standards such as ISO 13485, ISO 14971, UL/CE requirements, IEC 60601-1 and IEC 62304.Â
Familiarity with medical device cybersecurity principles and practices.Â
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