Robeauté is redefining the future of neurosurgery with self-propelled microrobots designed to navigate the human brain with unprecedented precision. Our technology makes it possible to reach deep brain regions that were previously inaccessible, without invasive surgery.

We have developed microrobots capable of travelling inside the brain to collect biopsies, deliver cancer drugs, and implant electrodes for neurological treatments.

Since our founding in 2017, we have filed 50+ patents and successfully tested our technology in living animals, with human clinical trials targeted for 2026/2027. We recently raised €27M in Series A funding from Plural, Cherry Ventures, Kindred Ventures, and Brainlab, fueling our next phase of growth.

As our manufacturing activities scale, we are looking for a Process Engineer to drive the industrialization of our microrobotic systems. This role focuses on developing robust, scalable, and reproducible mechanical manufacturing and assembly processes, ensuring a reliable transition from prototype to production in a highly regulated medtech environment.

You will develop and optimize precision assembly processes, define assembly flows, and design custom tooling and fixtures, with a strong focus on cleanroom operations. You play a key role in scaling manufacturing by establishing controlled, repeatable processes and maintaining strong oversight of product quality and critical parameters, also identifying and implementing automation opportunities to support scale-up.

Working closely with R&D, Quality, and Manufacturing, you will turn product designs into robust and manufacturable solutions. You will define manufacturing methods, build documentation, and ensure process reliability through validation and data-driven approaches.

• Strong expertise in the development, optimization, and industrialization of mechanical manufacturing and assembly processes, particularly for complex and miniaturized systems.
• Proven hands-on experience with precision assembly processes, including:
• • Definition and optimization of assembly sequences and workflows
  • Design and development of custom tooling, fixtures, and jigs
  • Assembly of complex systems involving tight tolerances and high repeatability
  • Integration of assembly operations in controlled environments (e.g., cleanroom)
• Solid experience with mechanical manufacturing processes, such as machining, precise assembly, bonding, polishing, welding (e.g., laser welding, adhesive bonding), with the ability to define and control critical process parameters.
• Experience in automation of manufacturing and assembly processes, including identification of automation opportunities, specification of equipment, and collaboration with automation or robotics teams.
• Strong involvement in methods engineering, including:
• • Proficiency with CAD software (e.g., SolidWorks, CATIA, or equivalent) for tooling design and manufacturing support
  • Definition of manufacturing processes and assembly flows
  • Development of work instructions
  • Implementation of Design for Assembly (DfA) and Design for Manufacturing (DfM) principles
• Hands-on experience with manufacturing equipment and tooling, including procurement, setup, qualification, and optimization.
• Proficiency in process characterization and statistical analysis, including DoE, SPC, process capability (Cp/Cpk), and measurement system analysis (R&R), to ensure process robustness and reproducibility.
• Strong experience in process and equipment validation (IQ/OQ/PQ), including definition of validation strategies and execution in compliance with regulatory expectations.
• Strong problem-solving skills using structured methodologies (e.g., root cause analysis, 5 Whys, Ishikawa, PDCA).
• Good understanding of cleanroom environments and constraints related to precision assembly and contamination control.
• Understanding of medical device regulatory frameworks (ISO 13485, GMP) and expectations related to process control, traceability, and validation.
• Ability to manage industrialization and process development projects, including planning, budget management, and cross-functional coordination.

• Strong analytical mindset with a high level of rigor in structuring, validating, and challenging technical approaches.
• Ability to solve complex, multidisciplinary problems using a pragmatic, data-driven, and solution-oriented approach.
• High level of ownership and autonomy, with the ability to operate effectively in a fast-paced and evolving environment.
• Proactive mindset, with the ability to anticipate risks, identify opportunities, and drive initiatives forward.
• Results-driven, with a focus on delivering robust, scalable, and compliant solutions.
• Strong collaboration skills, with the ability to work effectively across cross-functional teams (R&D, Quality, Manufacturing, Regulatory).
• Clear and structured communication, with the ability to convey complex technical topics to both technical and non-technical stakeholders.
• Excellent prioritization and organizational skills, with the ability to manage multiple high-impact topics simultaneously.
• Adaptability and resilience in a startup environment with shifting constraints and priorities.
• Technical leadership, with the ability to influence decisions, challenge assumptions, and align stakeholders around industrialization and process strategies.

• Master’s degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, or a related field.
• Minimum of 3 years of experience in the medical device industry, with a strong focus on mechanical manufacturing, assembly processes, or product industrialization.
• Proven experience working on Class III medical devices or similarly high-risk, highly regulated products, with exposure to clinical-stage or commercial manufacturing environments.
• Strong hands-on experience in mechanical assembly and manufacturing of complex systems, ideally involving high-precision or miniaturized components.
• Demonstrated experience in developing and validating assembly and mechanical manufacturing processes, including readiness for clinical use in regulated environments.
• Experience in designing and implementing assembly methods, including tooling, fixtures, and manufacturing documentation.
• Strong background in cleanroom manufacturing environments, with a solid understanding of contamination control and constraints related to precision assembly.
• Experience in scaling mechanical products or assemblies from prototype to production, in environments requiring high levels of traceability, validation, and documentation.

A Mission That Matters
Join a team developing life-changing technology. Our microrobots have the potential to impact over 1 billion patients with neurological conditions by enabling unprecedented access to the brain.

World-First Innovation
Work on pioneering microrobotic systems for brain diagnosis and treatment—minimally invasive, with maximum clinical impact.

An Exceptional Team
Collaborate with leading engineers, clinicians, and researchers at the forefront of medical robotics and neurotechnology.

Real Ownership
Join a well-funded deep-tech startup backed by top-tier investors. Take ownership of your domain, influence key technical decisions, and grow with the company.

• Health insurance — 60% covered by the company
• Meal vouchers — €9.25/day, 60% covered
• Transportation — 50% of commuting costs covered