Senior Staff Systems Engineer (HYBRID)

Posted 4 Days Ago
Be an Early Applicant
2 Locations
In-Office
103K-171K Annually
Senior level
Healthtech
The Role
Lead end-to-end design, development, and evaluation of complex medical device systems. Translate user needs into system requirements and architectures, decompose and allocate requirements across EE/ME/SW teams, drive integration, verification/validation, risk management, and documentation (DHF). Mentor engineers, conduct analytical trade-offs and performance studies, and ensure compliance with medical device standards.
Summary Generated by Built In
Work Flexibility: Hybrid

What You Will Do

  • Lead end-to-end design, development, and evaluation of complex medical device systems

  • Apply advanced engineering principles; mentor team members on best practices

  • Translate user needs into system requirements and scalable architectures

  • Define, decompose, and allocate requirements across multi-disciplinary teams (EE, ME, SW)

  • Lead concept phase activities and drive resolution of complex design issues

  • Conduct and lead analytical studies (trade-offs, optimization, performance, risk assessments)

  • Oversee system integration, verification, and validation activities

  • Drive product risk management, including failure analysis, safety requirements, and mitigations

  • Influence product and technology strategy through market, clinical, and customer insights

  • Ensure compliance with medical device standards; lead documentation (DHF) and cross-functional collaboration while mentoring and driving high-performance execution

What You Need (Minimum Required Qualifications)

  • Bachelor of Science in Software, Electrical, Mechanical, Systems, Biomedical Engineering or related degree & 6+ years of work experience

Preferred Qualifications (Strongly desired)

  • Proven experience designing, developing, and optimizing complex systems

  • Advanced proficiency in requirements management and system modeling methodologies

  • Strong ability to communicate complex technical concepts and plans to cross-functional teams

  • Hands-on experience with requirements management tools (Jama strongly preferred)

  • Experience with SysML and Model-Based Systems Engineering (MBSE) frameworks

  • Proficiency with SysML/MBSE modeling tools (e.g., Cameo, MagicDraw, Rhapsody)

  • Solid understanding of medical device standards, including ISO 13485 and ISO 14971

  


$102,600 - $171,000 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 of Science in Software, Electrical, Mechanical, Systems, Biomedical Engineering or related degree
  • 6+ years of relevant work experience
  • Proven experience designing, developing, and optimizing complex systems
  • Advanced proficiency in requirements management and system modeling methodologies
  • Hands-on experience with requirements management tools (Jama strongly preferred)
  • Experience with SysML and Model-Based Systems Engineering (MBSE) frameworks
  • Proficiency with SysML/MBSE modeling tools (Cameo, MagicDraw, Rhapsody)
  • Solid understanding of medical device standards, including ISO 13485 and ISO 14971

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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