Your mission
We are scientists, doctors, techies and humanity lovers, with the mission of pioneering real time precision neurology to cure brain-related disorders. INBRAIN harnesses the extraordinary material properties of Graphene, the world's thinnest and nobel-prize winning material, to build high resolution neural systems.
Our mission is to decode and modulate neural networks to restore people's lives.
As a
Human Factors and Usability Engineer
, you will lead and support human factors and usability engineering activities across INBRAIN's product portfolio, ensuring that products are safe, effective, and usable for their intended users and use environments. The role will work cross-functionally with Product, Engineering, Clinical, Quality, and Regulatory teams to plan, execute, and document usability engineering activities throughout development of INBRAIN's BCI platforms.
You will be at the forefront of bringing advanced healthcare solutions to market, making a tangible difference in people ?s lives worldwide.
Your profile
Main Responsibilities:
Work closely with Product, Engineering, Clinical, Regulatory, and Quality teams to ensure human factors considerations are integrated into development decisions.
Lead and support human factors engineering activities from early concept development through design validation
, including:
Define intended users, use environments, use scenarios, critical tasks, and success criteria to support robust usability engineering.
Identify
use-related risks, use errors, workflow challenges, and usability-related design issues, translating findings into clear recommendations for design improvement and risk mitigation.
Define, plan, execute,



and document formative and summative usability activities in line with applicable standards and regulatory expectations.
Create and
maintain
high-quality human factors documentation, including usability engineering plans, protocols, reports, risk-related inputs, traceability materials, and other design history file documentation.
Support regulatory submissions and audits by providing clear, structured, and inspection-ready human factors documentation.
Support the development of templates, processes, and SOPs that strengthen usability engineering practice within the QMS.
Mandatory Qualifications and Soft skills:
Degree in Human Factors, Ergonomics, Biomedical Engineering, Product Design, or
a related
field.
5+ years of relevant professional experience in human factors engineering
or usability engineering
for medical devices/pharma,
or other regulated healthcare
products.
Demonstrated ability to
independently structure, prioritize, and drive
complex human factors activities to completion, delivering high-quality outputs with minimal supervision.
Strong knowledge of the human factors engineering process for medical/
pharma devices
, including planning, execution, analysis, and reporting of formative and summative evaluations.
Strong understanding of IEC *, ISO *, FDA human factors expectations, and usability-related regulatory documentation.




Experience creating or contributing to usability engineering documentation within a design control / quality management system environment.
Fluency in English required (English is company language).
High degree of independence, ownership, and follow-through, with the ability to drive workstreams to completion in a fast-moving environment.
Proactive, inquisitive, and comfortable identifying gaps, asking clarifying questions, and improving ways of working.
Strong judgment in balancing user needs, patient/user safety, regulatory expectations, technical constraints, and broader product considerations.
Clear and objective communicator, able to translate usability findings into actionable recommendations for cross-functional stakeholders.
Collaborative working style, with the ability to
facilitate
discussions across Product, Engineering, Clinical, Quality, and Regulatory teams.
Structured, detail-oriented, and capable of producing documentation suitable for design history files, audits, and regulatory review.
Nice to have:
Experience supporting regulatory submissions and/or audits.
Experience with active implantable medical devices, neurostimulation systems, BCI platforms, or other complex hardware/software medical systems.
Experience working with clinical users and translating
workflow insights into design inputs, usability requirements, and risk mitigations.
Experience contributing to templates, SOPs, or process improvements within a regulated QMS environment.
Why us?
We are looking for someone who Is ready to proactively bring new ideas to the team, push boundaries, and constantly look for innovation. At INBRAIN we believe in shared success and diverse ways of thinking, here you'll learn

📌 Human Factors And Usability Engineer (Laza)
🏢 Inbrain Neuroelectronics
📍 Laza