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Human Factors and Usability Engineer (with Medical device or Pharma experience)


Job Location:

Barcelona - Spain

Monthly Salary: Not provided by the employer
Posted: 14 June 2026 (30+ days ago)
Application Deadline: 13 October 2026
Vacancies: 1 Vacancy

Job Summary

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 worlds thinnest and nobel-prize winning material to build high resolution neural systems.Our mission is to decode and modulate neural networks to restore peoples lives.

As a Human Factors and Usability Engineer you will lead and support human factors and usability engineering activities across INBRAINs 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 INBRAINs BCI platforms.

You will be at the forefront of bringing advanced healthcare solutions to market making a tangible difference in peoples 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.
    • Identifyuse-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 andmaintainhigh-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 ora relatedfield.
  • 5 years of relevant professional experience in human factors engineering or usability engineering (withinmedical devices/pharma industry only)
  • 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 62366 ISO 14971 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 tofacilitatediscussions 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 translatingworkflow 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 youll learn grow and advance in an innovative culture.


WHAT CAN WE OFFER TO YOU

  • Acollaborative environment where innovative ideas flourish and teamwork drives us forward. At INBRAIN we believe the power of collective intelligence is unique. You will be part of a team that thrives on open communication knowledge sharing and mutual respect.
  • Meaningful Work Impact:Our projects are not only exciting and challenging but also have a positive impact on the industry and society as a whole. Youll be part of a team that strives to create meaningful change.
  • Cutting-Edge Technology Exposure:Joining us means immersing yourself in the latest technologies and innovative solutions. Youll have access to state-of-the-art tools and resources fostering continuous learning and keeping your skills relevant in a rapidly evolving industry.
  • Competitive salary (according to your experience/skills)
  • Internal flexible compensation scheme
  • Private Health Insurance
  • Training bonus for professional development and access to Udemy platform
  • 23 vacation days per year
  • Christmas week off
  • Hybrid working modality

Applications must be submitted in English

At INBRAIN were not just offering a job were inviting you to be part of a transformative journey Are you ready to transform lives Join us!

#diverseandinclusive
We believe that a diverse and well-balanced workforce drives innovation. At INBRAIN we foster the inclusion of all people regardless of culture age gender sexual orientation identity and diverse abilities or any other status.
About us
At Inbrain Neuroelectronics we built our company around a simple belief: great science needs great people.

Our mission is to transform the treatment of neurological disorders through neuroelectronic therapies that are safer smarter and more humancentered. We work at the intersection of neuroscience engineering and advanced materials but what truly drives us is the impact our work can have on patients lives.


Our culture is grounded in Integrity Firstwe hold ourselves to the highest ethical standards because the people we serve deserve nothing less. We are Human Powered valuing empathy collaboration and the diverse perspectives that make our ideas stronger. We encourage everyone to think likeGame Changers challenging assumptions and pushing boundaries to unlock breakthroughs that once felt out of reach.


We act with Conscious Impact aware that every decisionfrom research to clinical translationshapes real futures. And we embrace aGrowth Mindsetcreating an environment where learning is continuous curiosity is celebrated and people are supported to stretch beyond their comfort zones.
At Inbrain youll join a team united by purpose and energized by possibility. If youre looking for a place where your talent can contribute to meaningful changeand where you can grow while helping others thriveyoull feel at home here.

Required Experience:

IC


About Company

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At Inbrain Neuroelectronics, we built our company around a simple belief: great science needs great people. Our mission is to transform the treatment of neurological disorders through neuroelectronic therapies that are safer, smarter, and more human‑centered. We work at the intersecti ... View more

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