Staff Systems Engineer, Robotics

Posted 16 Hours Ago
Be an Early Applicant
Portage, MI, USA
In-Office
103K-171K Annually
Mid level
Healthtech
The Role
Leads systems engineering for robotic surgical end effectors and electromechanical subsystems. Translates clinical and user needs into requirements, architectures, interfaces, and verification strategies. Coordinates integration across electrical, mechanical, software, controls, clinical, quality, and regulatory teams. Supports risk management, design history file documentation, system verification and validation, technical trade studies, and process improvements while mentoring engineers.
Summary Generated by Built In
Work Flexibility: Onsite

It's Time to Join Stryker!

Stryker is seeking a Staff Systems Engineer, Robotics to lead systems engineering activities for critical electromechanical components within a complex robotic medical platform.


In this role, you will serve as a systems engineering owner for robotic end effectors, including powered surgical tools and future attachments that interface directly with the robotic system. You will help translate user and clinical needs into system architecture and requirements, define interfaces across electrical, mechanical, and software disciplines, and guide the product from requirements development through integration and verification.


This role requires a highly collaborative engineer who can bring together input from multiple technical disciplines and maintain a system-level view throughout development.


What You Will Do
Systems Engineering
  • Own systems engineering activities for robotic end effectors and related electromechanical subsystems.
  • Translate user, clinical, and product needs into clear, verifiable system requirements and design inputs.
  • Develop and refine system architectures, interfaces, and functional requirements across electrical, mechanical, software, and controls disciplines.
  • Allocate and decompose system requirements to appropriate subsystems and engineering disciplines.
  • Lead technical trade studies, design assessments, performance analyses, and other systems engineering activities used to guide design decisions.
  • Support concept development and architecture definition for new end effectors, features, and product capabilities.

Requirements, Integration, and Verification
  • Establish and maintain requirements traceability throughout the product development lifecycle.
  • Develop system-level verification strategies and ensure requirements can be objectively verified.
  • Lead system integration activities across multiple engineering disciplines.
  • Investigate and help resolve complex system-level design and integration issues.
  • Lead or support system verification and validation activities as development progresses.
  • Contribute to product risk management and ensure appropriate linkage between risks, requirements, mitigations, and verification evidence.
  • Create and maintain engineering documentation supporting the Design History File.

Cross-Functional Leadership
  • Collaborate with Electrical, Mechanical, Software, Systems, Clinical, Quality, Regulatory, Manufacturing, and other stakeholders to ensure successful system development.
  • Support Voice of Customer activities and translate clinical workflows and customer needs into actionable engineering inputs.
  • Mentor engineers in systems engineering, requirements development, design controls, risk management, and verification practices.
  • Identify and implement improvements to systems engineering processes, tools, and practices.

What You Will Need
Minimum Qualifications
  • Bachelor of Science degree in Software Engineering, Electrical Engineering, Mechanical Engineering, Systems Engineering, Biomedical Engineering, or a related engineering discipline.
  • 4+ years of applicable engineering experience.

Preferred Qualifications
  • Experience developing or managing system requirements for complex products.
  • Experience working across multiple engineering disciplines such as electrical, mechanical, software, systems, or test.
  • Experience developing medical devices or other complex regulated products.
  • Experience with systems architecture, requirements development, decomposition, interface definition, integration, and verification.
  • Experience translating user or customer needs into system-level design inputs and requirements.
  • Experience developing verification strategies and supporting system integration and testing.
  • Experience with robotic systems, powered surgical tools, power tools, or other precision electromechanical products.
  • Experience with requirements management tools such as Jama, IBM DOORS, or equivalent.
  • Working knowledge of ISO 13485, ISO 14971, design controls, and medical device development practices.
  • INCOSE CSEP certification or equivalent systems engineering certification.
  • Strong communication and relationship-building skills with the ability to influence across technical disciplines.

  


  • $102,600 - $171,000 USD Annual

  


Travel Percentage: 10%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

Skills Required

  • Bachelor of Science degree in Software Engineering, Electrical Engineering, Mechanical Engineering, Systems Engineering, Biomedical Engineering, or a related engineering discipline
  • 4+ years of applicable engineering experience
  • Experience developing or managing system requirements for complex products
  • Experience working across electrical, mechanical, software, systems, or test engineering disciplines
  • Experience developing medical devices or other complex regulated products
  • Experience with systems architecture, requirements development, decomposition, interface definition, integration, and verification
  • Experience translating user or customer needs into system-level design inputs and requirements
  • Experience developing verification strategies and supporting system integration and testing
  • Experience with robotic systems, powered surgical tools, power tools, or precision electromechanical products
  • Experience with requirements management tools such as Jama, IBM DOORS, or equivalent
  • Working knowledge of ISO 13485, ISO 14971, design controls, and medical device development practices
  • INCOSE CSEP certification or equivalent systems engineering certification
  • Strong communication and relationship-building skills with the ability to influence across technical disciplines

Inari Medical Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.

  • Fair & Transparent Compensation Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
  • Healthcare Strength Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
  • Leave & Time Off Breadth Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.

Inari Medical Insights

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The Company
HQ: Irvine, CA
956 Employees

What We Do

Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.

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