Senior R&D Engineer, Software

Posted Yesterday
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Redwood City, CA, USA
In-Office
125K-145K Annually
Senior level
Healthtech
The Role
Develop embedded software for Class II/III pulsed-field electrosurgical medical devices, including automated testing and supporting tools. Lead software design controls, requirements, verification documentation, risk management, traceability, and design reviews. Collaborate with R&D, Quality, Regulatory, Clinical, and Operations teams to ensure product compliance with applicable medical device standards. Support design verification, sustaining engineering, complaint investigations, and continuous process improvements.
Summary Generated by Built In

About Galvanize Therapeutics

Galvanize is a biomedical platform company operating at the convergence of engineering, biology, and healthcare delivery, aiming to deliver life-changing solutions to patients and their doctors. We design and develop Pulsed Electric Field Systems to achieve meaningful and lasting therapeutic outcomes for patients.


About the role


The Senior R&D Engineer, Software will contribute to the development of new pulsed-field energy delivery electrosurgical devices. This role includes technical contribution to the design and development projects and execution of product verification and validation testing.


Qualifications


Education and Training:

  • Scientific degree in Software, Computer, Electrical, or Biomedical Engineering with consideration given to degree level combined with experience. Other degrees within the engineering discipline are acceptable with medical device experience.

Skills and Experience:

  • 5+ years of progressive experience in the design and development of software for Class II/III medical devices, preferably in ablation or energy delivery systems.
  • Proficiency in embedded software designs using C and C++ programming languages.
  • Experience with real-time operating systems used in embedded software.
  • Expertise in python, or other scripting languages, for data analysis.
  • Strong knowledge of Software Design Control and Risk Management requirements under 21 CFR Part 820, ISO 13485, and IEC 62304.
  • Experience with cybersecurity threat modeling, risk analysis and secure design practices
  • Proficient in authoring Risk Assessment Documents (e.g., Failure Mode and Effect Analysis Documents) and understanding risk analysis methodologies.
  • Strong attention to detail with a systematic approach to documentation and traceability.
  • Excellent communication and organizational skills; ability to manage multiple priorities.


What you'll do

  • Prepare and present clear, structured technical documentation and summaries for internal and external stakeholders.
  • Lead the development, documentation, and maintenance of Software Design Control elements including Software Requirements Specifications, Software Design Specifications, Design Verification protocols, test cases, and reports
  • Create and maintain Risk Management documentation in accordance with ISO 14971, including: Design, Use-Related, Process, and/or Software risk assessment for capital equipment and/or disposables.
  • Manage and maintain the Input/Output Trace Matrix, ensuring accurate linking of requirements, risks, and verification/validation activities.
  • Develop software for embedded devices, automated testing and supporting tools, ensuring that all design requirements are met. 
  • Collaborate cross-functionally with R&D, Quality, Regulatory, Clinical, and Operations teams to ensure cohesive development and regulatory alignment across the product lifecycle.
  • Participate in and/or lead formal design reviews, risk reviews, and test planning sessions.
  • Develop input and oversight for Design Verification (DV) testing activities to ensure adequate coverage of product requirements and risk mitigations.
  • Support updates to existing risk and design control documentation during design changes, sustaining engineering, or complaint investigations.
  • Ensure compliance with applicable regulatory standards including 21 CFR Part 820, ISO 13485, ISO 14971, and IEC 62304.
  • Assist in continuous improvement of the design control and risk management processes to improve efficiency and compliance.


This role pays between $125,000 and $145,000 per year, and your actual base pay will depend on your location, skills, qualifications, and experience.


Galvanize offers a robust benefits package to full-time employees, including medical, dental, and vision coverage, life insurance, short- and long-term disability protection, 401(k), and flexible paid time off.


Galvanize Therapeutics is an Equal Employment Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.


We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.

Skills Required

  • Scientific degree in Software, Computer, Electrical, Biomedical, or another engineering discipline; medical device experience may be required for other engineering degrees.
  • 5+ years of progressive experience designing and developing software for Class II/III medical devices, preferably ablation or energy delivery systems.
  • Proficiency with embedded software design using C and C++.
  • Experience with real-time operating systems used in embedded software.
  • Expertise in Python or other scripting languages for data analysis.
  • Knowledge of Software Design Control and Risk Management requirements under 21 CFR Part 820, ISO 13485, and IEC 62304.
  • Experience with cybersecurity threat modeling, risk analysis, and secure design practices.
  • Proficiency authoring risk assessment documents, including Failure Mode and Effect Analysis documents, and understanding risk analysis methodologies.
  • Strong attention to detail and systematic documentation and traceability practices.
  • Excellent communication and organizational skills with the ability to manage multiple priorities.

Galvanize Therapeutics Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Galvanize Therapeutics and has not been reviewed or approved by Galvanize Therapeutics.

  • Healthcare Strength — Healthcare coverage is described as comprehensive, with medical, dental, and vision available for employees and family members. Some public descriptions also reference fully paid health insurance in certain cases.
  • Leave & Time Off Breadth — Flexible paid time off and paid parental leave are advertised, alongside broader time-off elements in U.S. benefits listings. These offerings indicate wide-ranging leave options when team norms support utilization.
  • Flexible Benefits — Flexible work options and take‑as‑you‑need/unlimited PTO are featured across public materials. Such flexibility can add value if workloads allow for regular use.

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The Company
HQ: San Carlos, CA
111 Employees
Year Founded: 2015

What We Do

Galvanize Therapeutics is developing therapies to deliver life-changing healthcare solutions to patients and their doctors at the convergence of biology, engineering, and care delivery.

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