Back to results

Closed listing

Staff R&D Engineer

  • Waltham, MA, United States

US20: $107,200 - $178,600 USD Annual View the U.S. work location and transparency guide to find the pay range for your location.

This opening has closed.

The original listing is kept below for reference.

Job details

Pay
US20: $107,200 - $178,600 USD Annual View the U.S. work location and transparency guide to find the pay range for your location.
Experience
Minimum 4 years of engineering work experience.
Posting language
English
Posted

Similar jobs hiring now

Search current openings

Original job description

Archived listing. The details below describe a past opening.

Join Stryker’s Amplitude Vascular Systems (AVS) team in Waltham, Massachusetts as a Staff R&D Engineer - Systems Engineering. In this role, you’ll be supporting the development of complex medical devices from concept through commercialization, working across software, electrical, and mechanical systems. You will translate stakeholder and clinical needs into system requirements and guide system architecture, interface management, risk management, integration, verification, and validation across multidisciplinary engineering teams.

What you will do

  • Translate user, stakeholder, and clinical needs into clear system-level requirements and design inputs for complex medical devices.
  • Develop and refine system architectures, interfaces, requirements, and verification strategies across mechanical, electrical, and software disciplines.
  • Allocate and decompose system requirements using modeling, simulation, engineering budgets, and mathematical techniques.
  • Support concept-phase engineering activities, including trade studies, sensitivity analyses, optimization studies, performance assessments, and design assessments.
  • Drive system integration, verification, and validation activities and resolve complex product design issues using engineering analysis and technical judgment.
  • Contribute to product risk management activities and apply applicable medical device standards, design controls, and risk management practices throughout development.
  • Create and refine engineering documentation, including Design History File documentation, and mentor team members on development procedures and applicable industry standards.
  • Collaborate with clinical, quality, regulatory, manufacturing, and engineering partners, including supporting Voice of Customer activities with clinicians, to identify technical risks and advance projects through development and launch.

What you will need Required qualifications

  • Bachelor of Science degree in Software Engineering, Electrical Engineering, Mechanical Engineering, Systems Engineering, Biomedical Engineering, or a related engineering discipline.
  • Minimum 4 years of engineering work experience.

Preferred qualifications

  • Experience developing and optimizing system requirements, system designs, and verification strategies.
  • Experience using requirements management software, preferably Jama.
  • Experience with Systems Modeling Language (SysML) and Model-Based Systems Engineering (MBSE) methods and tools.
  • Knowledge of ISO 13485 and ISO 14971 requirements and their application to medical device development.
  • Experience working with software and/or electrical systems.
  • Familiarity with C++, MATLAB, or scripting languages.

US20: $107,200 - $178,600 USD Annual View the U.S. work location and transparency guide to find the pay range for your location.

More about this job

Skills

  • Medical devices
  • Mechanical systems
  • Risk management
  • ICT system integration
  • Documentation
  • Electrical engineering
  • Mechanical engineering
  • Biomedical engineering
  • C++
  • The MathWorks MATLAB

Report this job