Staff Engineer

Posted 2 Days Ago
Be an Early Applicant
Bengaluru, Bengaluru Urban, Karnataka, IND
In-Office
Mid level
Healthtech
The Role
Designs, develops, tests, evaluates, and verifies software components for medical devices. Leads advanced prototyping, research, requirements analysis, architecture, coding, testing, documentation, and design tradeoff decisions. Supports software estimates, code reviews, regulatory compliance, design controls, risk management, and Design History File development. Collaborates with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management teams throughout product development, from concept through launch.
Summary Generated by Built In
Work Flexibility: Hybrid

What you will do:
Technical Responsibilities:
• Conduct or design advanced prototyping and testing
• Conduct advanced problem solving, identify potential solutions, and evaluate them against component and sub-system requirements
• Conduct and design research and studies to support advanced product design
• Translate user needs to design inputs/specifications and produce advanced component and sub-system level designs
• Analyze and correct complex product design issues, using independent judgment
• Independently balance design tradeoffs while designing a component of the system
• Develop and design software systems per requirements and architecture defined
• Code development time/resource estimation to support projects
• Generate and review the necessary documents to support the project. (requirements/design/architecture/bugs/test)
Business Responsibilities:
• Advance solutions by applying in-depth knowledge of customer needs, market and competitive offerings
• Apply detailed knowledge of clinical procedures to author design inputs
• Support Voice of Customer sessions internally and with clinicians
• Demonstrate developing financial acumen
Med Device Compliance:
• Be proficient with and mentor others in usage of industry standards, including design requirements and test strategies per applicable regulations
• Lead creation and refinement of engineering documentation, such as the Design History file
• Follow and mentor others on R&D procedures like design controls and risk management, per the Quality Management System
General Responsibilities:
• Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success as a leader on the team
• Identify and support the creation of or improvements to procedures, policies, processes, systems, and technology
• Support and execute segments of complex product development to advance projects through the design /development/launch process
• Contribute to product development from concept through release
• Deliver high quality results with passion, energy and drive to meet business priorities
• Build relationships and influence across the engineering groups within the business
• Design, develop, modify, evaluate and verify software components for medical devices
• In code reviews apply design principals, coding standards and best practices
Minimum Qualifications (Required):
• Bachelor's degree in Software Engineering/ Computer Science or related discipline & 4+ years of work experience
Preferred Qualifications (Strongly desired):
Technical Skills:
• Knowledgeable programming skills. Design new components applying various concepts design concepts and patterns
Design and Development Skills:
• Knowledgeable with integrated development environments (IDE) for projects
• Knowledgeable with tools for static/dynamic analysis, memory management, code coverage and techniques for analyzing software
• Knowledge in integration and deployment processes
Software Process Skills:
• Software Development Life Cycle processes
• Knowledge in creating estimates for code implementation time/resource for assigned tasks and projects
• Knowledge from using Application Lifecycle Management /Traceability tools.
• Knowledge of regulatory and compliance standards applied to the SDLC (Software Development Life Cycle)

Travel Percentage: None

Skills Required

  • Bachelor's degree in Software Engineering, Computer Science, or a related discipline
  • 4+ years of work experience
  • Knowledgeable programming skills, including designing components using design concepts and patterns
  • Experience with integrated development environments for software projects
  • Knowledge of static and dynamic analysis, memory management, code coverage, and software analysis techniques
  • Knowledge of software integration and deployment processes
  • Knowledge of Software Development Life Cycle processes
  • Experience creating code implementation time and resource estimates
  • Knowledge of Application Lifecycle Management and traceability tools
  • Knowledge of regulatory and compliance standards applied to the Software Development Life Cycle

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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