Principal Engineer, Systems Engineering

Posted An Hour Ago
Be an Early Applicant
2 Locations
In-Office
118K-197K Annually
Senior level
Healthtech
The Role
Leads systems engineering for complex medical device products, including system architecture, technical strategy, requirements development, traceability, verification planning, integration, risk assessment, and design decisions. Translates customer, clinical, and business needs into system requirements while coordinating software, electrical, mechanical, quality, regulatory, and clinical stakeholders. Guides multidisciplinary product development from concept through verification, ensures compliance with design controls, evaluates emerging technologies, and influences global teams without direct authority.
Summary Generated by Built In
Work Flexibility: Hybrid or Onsite

Stryker is seeking a dynamic and visionary product development leader with a proven track record of leading large, complex product development programs through the application of systems engineering principles. As the technical quarterback, this individual will drive alignment, collaboration, and execution across a multidisciplinary global product line, ensuring teams work cohesively toward shared objectives while delivering innovative solutions that improve patient care.


As medical technologies continue to evolve, our products must operate seamlessly within broader healthcare ecosystems and enabling technology platforms. This leader will be responsible for defining and overseeing system-level architectures, ensuring robust integration across hardware, software, data, connectivity, and partner technologies. They will champion a systems-thinking approach, proactively identify opportunities and risks, and ensuring our products deliver a seamless user experience while supporting the future needs of a connected healthcare environment.


The ideal candidate combines deep technical expertise with exceptional leadership, influencing stakeholders across functions, geographies, and organizational levels to bring complex systems and product visions to life.


https://www.stryker.com/us/en/nse.html


What You Will Do


  • Lead system architecture, technical strategy, and integration activities for complex medical device products and platforms.
  • Translate customer, clinical, and business needs into system-level requirements and drive alignment across software, electrical, and mechanical engineering teams.
  • Lead requirements development, allocation, traceability, and verification planning throughout the product lifecycle.
  • Drive system-level decision making, architecture reviews, tradeoff analyses, and risk assessments.
  • Lead cross-functional product development efforts from concept through verification, ensuring delivery of safe, reliable, and high-quality solutions.
  • Partner with Quality, Regulatory, Clinical, and Engineering stakeholders to ensure compliance with design controls and applicable standards.
  • Identify, assess, and mitigate product development risks while promoting a risk-based development approach.
  • Evaluate emerging technologies and recommend new capabilities, platforms, and solutions that support future customer needs.
  • Build alignment across global stakeholders and influence design direction without direct authority.

What You Will Need (Required Qualifications)


  • Bachelor’s degree in Systems, Electrical, Mechanical, Software, Biomedical Engineering, or a related engineering discipline.
  • 8+ years of relevant engineering experience in product development, systems engineering, or technical leadership roles.
  • Experience developing products within a regulated industry environment.

Preferred Qualifications


  • Medical device product development experience.
  • Experience leading system architecture and integration activities for complex, multidisciplinary products.
  • Knowledge of requirements management, verification, and system-level risk management.
  • Experience with ISO 13485, ISO 14971, FDA Design Controls, or similar regulatory frameworks.
  • Experience with requirements management tools such as Jama, DOORS, or Polarion.
  • Experience with Model-Based Systems Engineering (MBSE) and SysML.
  • Experience developing connected products, digital health solutions, or integrated healthcare technologies.
  • Experience mentoring engineers and leading design efforts across cross-functional teams.

  


$118,000 - $196,700 USD Annual

  


Travel Percentage: 20%

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’s degree in Systems, Electrical, Mechanical, Software, Biomedical Engineering, or a related engineering discipline
  • 8+ years of relevant engineering experience in product development, systems engineering, or technical leadership roles
  • Experience developing products within a regulated industry environment
  • Medical device product development experience
  • Experience leading system architecture and integration activities for complex, multidisciplinary products
  • Knowledge of requirements management, verification, and system-level risk management
  • Experience with ISO 13485, ISO 14971, FDA Design Controls, or similar regulatory frameworks
  • Experience with requirements management tools such as Jama, DOORS, or Polarion
  • Experience with Model-Based Systems Engineering (MBSE) and SysML
  • Experience developing connected products, digital health solutions, or integrated healthcare technologies
  • Experience mentoring engineers and leading design efforts across cross-functional teams

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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