Senior Staff Systems Engineer - Data

Posted Yesterday
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Fort Lauderdale, FL, USA
In-Office
118K-197K Annually
Senior level
Healthtech
The Role
Leads data architecture and management for robotic medical-device platforms. Defines data structures, interfaces, requirements, models, governance, security, interoperability, and lifecycle strategies across clinical and engineering domains. Drives cross-functional architecture, system integration, verification, validation, risk analysis, and regulatory compliance. Translates clinical, customer, business, and regulatory needs into system requirements and implementation roadmaps while mentoring engineers and supporting product development.
Summary Generated by Built In
Work Flexibility: Hybrid


What You Will Do:

 The Senior Staff Systems Engineer will be responsible for the data architecture and management framework for the robotic platform. This role will lead the definition and implementation of data architectures supporting clinical applications, modular utility tools and platform services across R&D, service, clinical, and insight intra-operative and post-operative use cases. The role will lead the development of data logging capabilities enabling consistent, traceable, secure, and interoperable collection and management of data across the machine, utility, and clinical domains.


  • Lead the research, design, development, and evaluation of complex robotic and medical device systems, including platform data architecture and data management capabilities.
  • Translate clinical, customer, regulatory, and business needs into system requirements, architecture decisions, and implementation roadmaps.
  • Define and maintain system and data architecture artifacts, including requirements models, interface definitions, data flows, and test architectures.
  • Drive requirements decomposition, system modeling, and cross-functional integration across software, electrical, mechanical, and systems engineering teams.
  • Lead system verification, validation, and analytical activities, including trade studies, performance assessments, optimization studies, and risk analyses.
  • Establish governance for data structures, interfaces, security, interoperability, and lifecycle management across platform and clinical data domains.
  • Guide resolution of complex design challenges, facilitate architecture reviews, and support product development through release in compliance with medical device regulations and standards.
  • Mentor engineers, contribute to technology strategy and innovation, and partner with customers and cross-functional stakeholders to advance product and platform capabilities.


What You Will Need:

Required Qualifications:

  • Bachelor of Science in Software, Electrical, Mechanical, Systems, or Biomedical Engineering & 6+ years of work experience
  • Experience in developing and optimizing complex systems
  • Experience leading cross-functional architecture decisions across systems and software domains.
  • Experience with real-time and event-driven data flows.
  • Ability to translate clinical, service, R&D, regulatory, and business use cases into system-level data needs, architecture decisions, requirements, and implementation roadmaps.
  • Demonstrated experience defining data architectures, data products, information models, schemas, metadata, interfaces, and lifecycle strategies for complex system-of-systems products.
  • Working knowledge of data governance, privacy, cybersecurity, and regulated-data practices, including PII/PHI classification, labeling, retention, access, and secure transfer.

Preferred Qualifications:

  • Advanced knowledge of Requirements Management Tools and System Modeling Tools
  • Knowledge of ISO 13485 and ISO 14971.     

 

Must be legally authorized to work in the U.S. and not require employment-based sponsorship now or in the future.
 

  


:

  • $118,000 - $196,700 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 in Software, Electrical, Mechanical, Systems, or Biomedical Engineering
  • 6+ years of work experience
  • Experience developing and optimizing complex systems
  • Experience leading cross-functional architecture decisions across systems and software domains
  • Experience with real-time and event-driven data flows
  • Ability to translate clinical, service, R&D, regulatory, and business use cases into system-level data needs, architecture decisions, requirements, and implementation roadmaps
  • Experience defining data architectures, data products, information models, schemas, metadata, interfaces, and lifecycle strategies for complex system-of-systems products
  • Working knowledge of data governance, privacy, cybersecurity, and regulated-data practices, including PII/PHI classification, labeling, retention, access, and secure transfer
  • Advanced knowledge of requirements management tools and system modeling tools
  • Knowledge of ISO 13485 and ISO 14971
  • Legally authorized to work in the United States without requiring employment-based sponsorship now or in the future

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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