Robeauté is redefining the future of brain therapies through the first microrobotic platform designed to navigate the human brain with unprecedented precision. This new generation of medical microrobots will be able to diagnose, treat, and monitor the brain from within, overcoming the persistent limitations in treating neurological diseases that affect more than one in three people worldwide.Since its founding in 2017, Robeauté has filed more than 50 patent applications. We recently raised €27 million in a Series A round led by Plural, Cherry Ventures, Kindred Ventures, and Brainlab, fueling our next phase of growth.Now, as we scale, we are looking for a System V&V Engineer to define and lead robust system design verification studies across our medical device portfolio, ensuring regulatory compliance and engineering excellence. What you’ll do System Product/Device Verification Define the system-level verification strategies, ensuring full traceability to user and design requirements in compliance with our Quality Management System and design control procedures based on ISO 13485, ISO 14971 and FDA rules and guidelines. Develop and lead functional and safety testing according to the system verification strategy, ensuring coverage and alignment with design inputs and regulatory standards (e.g., compliance with ISO 10993 series, ISO 11607, System functional integration and robustness tests) Ensure that verification studies on the hardware and software components (e.g., based on ISO 60601-1 for electrical safety, 62304 for medical device software, IEC 80001-5-1 and IEC 82304-1 for cybersecurity) owned by R&D team are integrated in the system verification strategy.Collaborate with cross-functional teams to analyze test results, identify root causes of system issues, define corrective and preventive actions. Support validation and design transfer activities, ensuring the integrity of verification evidence in the Design History File (DHF). Cross-Functional Collaboration Collaborate closely with system, software and hardware engineering teams to ensure seamless integration of all subsystems into a unified, high-performance product. Interface with Quality Assurance, Regulatory Affairs, and Clinical teams to ensure verification deliverables meet regulatory submission and audit requirements. Participate in design reviews, risk assessments, and usability evaluations, providing system-level insight into potential design or integration issues. Contribute to continuous improvement of verification processes, test automation strategies, and system-level test methodologies. Training & Process Leadership Act as a leader within the System team, guiding integration of best practices and alignment across projects regarding system verification testing. Provide training and mentorship to engineers, project leads, and technical managers on regulatory expectations about design verification testing. Support cross-functional alignment on technical decisions, risk mitigation strategies, and verification priorities. Continuously monitor industry trends and evolving standards to adapt and improve internal design control processes, with specific attention to testing procedures. Promote a culture of rigor, traceability, and regulatory discipline across the product lifecycle. RequirementsRequirements Technical Skills Working knowledge of ISO 13485, ISO 14971, ISO 10993, ISO 11607 and FDA 21 CFR 820. Hands-on experience with ALM tools (e.g., Jama, Matrix Requirements), statistical analysis. Familiarity with ISO 60601-1 and collaterals standards, ISO 62304, and cybersecurity standards (e.g., FDA premarket guidance) is a plus. Personal Attributes Analytical, methodical, and rigorous, with a strong process orientation. Excellent communicator and trainer, able to influence cross-functional teams. Pragmatic and proactive, with a commitment to documentation and compliance. Comfortable working in a multidisciplinary and fast-paced environment. Education and Experience Bachelor’s or Master’s degree in Electrical Engineering, Biomedical Engineering, Systems Engineering, or related field. 5+ years of experience in system integration, verification, and design control within the medical device industry. Proven ability to develop and maintain verification documentation (V&V plans, test protocols, reports, and traceability) and execute design verification strategies. BenefitsA Mission That Matters: Join a team developing life-changing technology. Our microrobots have the potential to help over 1 million patients with neurological conditions.World-First Innovation: Work on pioneering microrobots that navigate the brain for diagnosis and treatment—minimally invasive, maximum impact.An Exceptional Team: Collaborate with leading engineers, clinicians, and researchers pushing the boundaries of medical robotics and neurotechnology.Real Ownership: Join a well-funded deeptech startup backed by top investors. Shape your domain, drive strategic decisions, and grow with us.Benefits: Health Insurance — We happily cover 60% of the cost.Meal Vouchers — €9.25 per day, We happily cover 60% of the cost.Transportation Reimbursement — 50% of your commuting costs covered.
Robeauté is redefining the future of brain therapies through the first microrobotic platform designed to navigate the human brain with unprecedented precision. This new generation of medical microrobots will be able to diagnose, treat, and monitor the brain from within, overcoming the persistent limitations in treating neurological diseases that affect more than one in three people worldwide.
Since its founding in 2017, Robeauté has filed more than 50 patent applications. We recently raised €27 million in a Series A round led by Plural, Cherry Ventures, Kindred Ventures, and Brainlab, fueling our next phase of growth.
Now, as we scale, we are looking for a System V&V Engineer to define and lead robust system design verification studies across our medical device portfolio, ensuring regulatory compliance and engineering excellence.
What you’ll do
System Product/Device Verification
- Define the system-level verification strategies, ensuring full traceability to user and design requirements in compliance with our Quality Management System and design control procedures based on ISO 13485, ISO 14971 and FDA rules and guidelines.
- Develop and lead functional and safety testing according to the system verification strategy, ensuring coverage and alignment with design inputs and regulatory standards (e.g., compliance with ISO 10993 series, ISO 11607, System functional integration and robustness tests)
- Ensure that verification studies on the hardware and software components (e.g., based on ISO 60601-1 for electrical safety, 62304 for medical device software, IEC 80001-5-1 and IEC 82304-1 for cybersecurity) owned by R&D team are integrated in the system verification strategy.
- Collaborate with cross-functional teams to analyze test results, identify root causes of system issues, define corrective and preventive actions.
- Support validation and design transfer activities, ensuring the integrity of verification evidence in the Design History File (DHF).
Cross-Functional Collaboration
- Collaborate closely with system, software and hardware engineering teams to ensure seamless integration of all subsystems into a unified, high-performance product.
- Interface with Quality Assurance, Regulatory Affairs, and Clinical teams to ensure verification deliverables meet regulatory submission and audit requirements.
- Participate in design reviews, risk assessments, and usability evaluations, providing system-level insight into potential design or integration issues.
- Contribute to continuous improvement of verification processes, test automation strategies, and system-level test methodologies.
Training & Process Leadership
- Act as a leader within the System team, guiding integration of best practices and alignment across projects regarding system verification testing.
- Provide training and mentorship to engineers, project leads, and technical managers on regulatory expectations about design verification testing.
- Support cross-functional alignment on technical decisions, risk mitigation strategies, and verification priorities.
- Continuously monitor industry trends and evolving standards to adapt and improve internal design control processes, with specific attention to testing procedures.
- Promote a culture of rigor, traceability, and regulatory discipline across the product lifecycle.
Requirements
Requirements
Technical Skills
- Working knowledge of ISO 13485, ISO 14971, ISO 10993, ISO 11607 and FDA 21 CFR 820.
- Hands-on experience with ALM tools (e.g., Jama, Matrix Requirements), statistical analysis.
- Familiarity with ISO 60601-1 and collaterals standards, ISO 62304, and cybersecurity standards (e.g., FDA premarket guidance) is a plus.
Personal Attributes
- Analytical, methodical, and rigorous, with a strong process orientation.
- Excellent communicator and trainer, able to influence cross-functional teams.
- Pragmatic and proactive, with a commitment to documentation and compliance.
- Comfortable working in a multidisciplinary and fast-paced environment.
Education and Experience
- Bachelor’s or Master’s degree in Electrical Engineering, Biomedical Engineering, Systems Engineering, or related field.
- 5+ years of experience in system integration, verification, and design control within the medical device industry.
- Proven ability to develop and maintain verification documentation (V&V plans, test protocols, reports, and traceability) and execute design verification strategies.
Benefits
A Mission That Matters: Join a team developing life-changing technology. Our microrobots have the potential to help over 1 million patients with neurological conditions.
World-First Innovation: Work on pioneering microrobots that navigate the brain for diagnosis and treatment—minimally invasive, maximum impact.
An Exceptional Team: Collaborate with leading engineers, clinicians, and researchers pushing the boundaries of medical robotics and neurotechnology.
Real Ownership: Join a well-funded deeptech startup backed by top investors. Shape your domain, drive strategic decisions, and grow with us.
Benefits:
- Health Insurance — We happily cover 60% of the cost.
- Meal Vouchers — €9.25 per day, We happily cover 60% of the cost.
- Transportation Reimbursement — 50% of your commuting costs covered.
At Robeauté we are developing a really small microrobot for novel therapies in hard-to-reach areas of the body. Designed specifically for the brain, at the service of neurosurgeons, our microrobot will be able to freely navigate in other complex regions of the body to perform biopsies, collect precise anatomically localized data and deliver therapies on site, at the right dosage. We are accompanying a major shift from robotic surgery to microrobotic surgery, for greater precision, better results and bold new therapies to tackle global diseases affecting more than a billion people worldwide.Our microrobot will light a spark in the minds of medical practitioners and scientists around the world, allowing them to imagine and create more effective treatments, to be delivered locally.We are a pluridisciplinary and multicultural team of passionate, skilled, supportive and creative people, at the crossroads of microrobotics, engineering and medicine.
We work with phenomenal medical centers and university labs in Europe and the United States. Our team is growing and we are constantly on the lookout for highly-talented individuals. Working with us means working on something that has never been done before, so you will be challenged - and you will be supported.
We are team players, with both classical and atypical backgrounds, so unconventional thinking is welcome and good communication skills are a must.We are based in Paris, France.
At Robeauté we are developing a really small microrobot for novel therapies in hard-to-reach areas of the body.
Designed specifically for the brain, at the service of neurosurgeons, our microrobot will be able to freely navigate in other complex regions of the body to perform biopsies, collect precise anatomically localized data and deliver therapies on site, at the right dosage.
We are accompanying a major shift from robotic surgery to microrobotic surgery, for greater precision, better results and bold new therapies to tackle global diseases affecting more than a billion people worldwide.
Our microrobot will light a spark in the minds of medical practitioners and scientists around the world, allowing them to imagine and create more effective treatments, to be delivered locally.
We are a pluridisciplinary and multicultural team of passionate, skilled, supportive and creative people, at the crossroads of microrobotics, engineering and medicine.
We work with phenomenal medical centers and university labs in Europe and the United States.
Our team is growing and we are constantly on the lookout for highly-talented individuals. Working with us means working on something that has never been done before, so you will be challenged - and you will be supported.
We are team players, with both classical and atypical backgrounds, so unconventional thinking is welcome and good communication skills are a must.
We are based in Paris, France.
