• Operate equipment involved in medical device fabrication, including ICP-RIE, optical microscopy, wet etching, photolithography, and more.
• Record inspection data, prepare reports, and promptly notify supervisors of any deviation. Ensure outgoing product quality in accordance with guidelines. Assist with traceability to ensure full compliance with regulatory requirements.
• Perform routine tasks with accuracy, adhering strictly to established methodologies.
• Provide comprehensive technical support to maintain effective manufacturing operations.
• Execute duties following Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and safety-compliant protocols.
• Work in compliance with SOPs, work instructions, and established process recipes. Participate in training and qualification activities to maintain team competency and adherence to protocols.
• Maintain equipment calibration, cleanliness, and  service ability; ensure the safe disposal of waste.
• Supervise materials and inventory levels to ensure uninterrupted operations, proactively managing stock, coordinating with supply chain teams, and verifying availability of critical components for timely execution of cleanroom processes.
• Independently organize and oversee cleanroom activities, including scheduling, workflow optimization, and coordination with cross-functional teams to ensure operational efficiency.

• Fluency in English required (company main language).
• Bachelor technical degree (engineering, materials, chemical, mechanical, electrical or related field)
• 2-3 years of Laboratory or Cleanroom experience (preferably within company setting).
• Capable of working independently with minimal supervision.
• Strong organizational skills with the ability to prioritize tasks, manage time effectively, and adapt to shifting priorities. Able to meet tight deadlines and handle multiple responsibilities simultaneously.
• High attention to detail, with a strong focus on quality, accuracy, sterility, and adherence to aseptic techniques.
• Maintains a positive attitude and works well both independently and collaboratively in a team environment.

• Experience with thin films and/or semiconductor manufacturing and/or assembly is a strong plus.
• General knowledge of microfabrication processes within the semiconductor industry such as: reactive ion etching; wet etching techniques; photolithography; metal deposition is a strong plus.
• Experience in quality control for medical devices or another highly regulated environment is a nice to have.
• Good understanding of Spanish is a nice to have.

• A collaborative 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. You'll 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. You'll 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
• While we offer flexible working modality, because of the nature of this position, this will be an office-based position in Bellaterra.

• Develop and maintain high-quality training materials for the use of our product in clinical settings, covering integration with other clinical equipment and workflows.
• Deliver training sessions to partner clinicians, hospital staff, and customers. 
• Provide on-site and remote support during clinical procedures and studies.
• Troubleshoot technical and clinical issues in collaboration with physicians and internal teams. 
• Support the execution of clinical studies in investigational sites. 
• Coordinate with clinical teams and sites to ensure smooth study conduct. 
• Contribute to protocol implementation and adherence in the field.
• Translate field feedback into actionable insights for product and clinical teams. 
• Act as a key point of contact and build strong relationships with clinical partners and KOLs.
• Represent the company in clinical environments with professionalism and credibility.

• Degree in biomedical engineering, clinical engineering, or related field.
• 5 years experience in a clinical or field-facing role specifically within medtech industry (industry experience is a must).
• Strong understanding of medical device usage in clinical environments.
• Excellent communication and training skills.
• Fluency in English required (English is company language). 
• Ability to work cross-functionally with technical and clinical teams.
• Willingness to travel frequently and work in hospital settings (30-50%). Position is supporting product release in clinics, intensive travels to hospital is a must.
• Strong problem-solving skills in high-pressure clinical settings.
• Ability to translate complex technical concepts into practical clinical guidance.
• Autonomy and adaptability in fast-paced environments.
• High level of professionalism when interacting with clinicians and KOLs.
• Hands-on mindset with attention to detail and patient safety.
• Strong ability to persuade and represent the company externally, along with the capacity to adapt communication styles effectively to different audiences.
• Business development mindset.

• Experience in intraoperative environments (e.g., operating room support). 
• Exposure to neurology, neurosurgery, or neurotechnology. 
• Experience supporting clinical trials or investigational studies. 
• Familiarity with hospital workflows and multi-device environments.

• A collaborative 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. You'll 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. You'll 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

• Support the planning and coordination of clinical investigations and investigator-initiated studies.
• Assist with study start-up, study tracking, and operational activities.
• Coordinate interactions with CROs, vendors, and investigational sites.
• Manage and mantain study documentation and Trial Master Files (TMF).
• Contribute to compliance with ICH-GCP, ISO 14155, MDR, and internal procedures.
• Support clinical data review and data quality activities in collaboration with CRO, as applicable.
• Prepare study status updates, reports, and operational metrics.
• Contribute to the development and continuous improvement of clinical SOPs and operational processes.

• Bachelor’s degree in Life Sciences, Biomedical Engineering, or a related field.
• +2 years of experience in clinical research, clinical trial coordination, data management, or a related role.
• Understanding of clinical research processes and ICH-GCP principles.
• Excellent written and verbal communication skills in English (company culture language).
• Strong organisational and coordination skills.
• Ability to manage multiple priorities and deadlines, attention to details.
• Effective communication and stakeholder management skills.
• Proactive, collaborative, and adaptable approach.

• Exposure to Clinical Data Management or EDC systems.
• Experience in medical device clinical research.
• Familiarity with ISO 14155 and MDR requirements.
• Experience working with CROs, vendors, and investigational sites.

• A collaborative 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. You'll 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. You'll 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

• Database Architecture 
  • Design and optimize relational and non-relational database schemas for new and existing applications. 
  • Implement data storage solutions that maximize performance, scalability, and reliability. 
  • Collaborate with developers to optimize storage, performance and data structures. 
  • Oversee database security, backup, recovery, and maintenance strategies.
•  Data Architecture 
  • Develop and maintain the organization’s enterprise data model and data flow architecture. 
  • Aware of data quality, governance, and compliance across all systems. 
•  Collaboration & Strategy 
  • Work closely with developers, AI/ML engineers, data engineers, analysts, and business stakeholders to align data infrastructure with business needs. 
  • Evaluate and recommend future database technologies, cloud solutions, and analytics platforms. 
  • Establish best practices for data management, storage, and access across the organization. 

• Bachelor’s or Master’s degree in Computer Science, Information Systems, or related field.
• 5+ years of experience in database design, administration, or data architecture. 
• Strong expertise in SQL, NoSQL, and relational database management systems  
• Knowledge of data governance, quality, and compliance frameworks. 
• Strong analytical, problem-solving, and communication skills. 
• Fluency in English required (English is company language).
• Familiarity with cloud platforms (AWS, Azure, GCP). 
• Familiarity with cluster/virtualization technologies as Docker containers and/or Kubernetes is a plus. 
• Ability to design end-to-end data solutions, from database schema to enterprise-wide data flow. 
• Experience in optimizing query performance and storage.
• Strong problem-solving skills and attention to details.
• Ability to work effectively in a team and communicate ideas clearly.
• Adaptability and willingness to learn new technologies.
• Strong communication skills (ability to work with non-technical people and translate complicated technical challenges).

• Understanding of machine learning processes

• A collaborative 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. You'll 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. You'll 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

• Own functional roadmaps in the electronics area for capability growth, tooling, innovation and product delivery.
• Ensure early engagement and alignment with core suppliers to secure times, innovation inputs and compliance.
• Build and maintain strong and innovative partnerships with suppliers to deliver on time and at cost.
• Ensure that the technical standards at the fore front of the field are maintained across all products.
• Ensure fast, expert execution support is provided to the Core Teams.
• Develop, maintain and enforce functional standards, procedures and compliance frameworks.
• Advance tools, methods and processes within the area of scope to accelerate product delivery without compromising quality.
• Manage and update curated,validated and innovative supplier portfolio aligned with product roadmaps.
• Capture and apply cross-product learnings to shorten future delivery cycles.
• Resource planning of the electronics function, sharing best practices and driving the vision of the function.
• Formulate objectives and set goals for all the members of the electronics team, monitoring and following up of performance and motivation.
• Arrange and structure resources and tasks within the team to ensure implementation of plans.
• Provide direction, technical support where needed, motivation and guidance towards achieving product goals.
• Collaboratively recruits and trains employees to ensure that the organization has the right talent to achieve its goals. This also involves creating an environment that promotes employee growth and development.

• A system-thinking attitude identifying areas of potential improvement and developing plans to address these; Team oriented, a sparring partner to colleagues in other disciplines.
• BSc or MSc in electronics Engineering with at least 5 years of work experience in a relevant industrial setting (regulated environment; MedTech is a strong plus) with proven experience executing a full development cycle. Experience in developing multidisciplinary medical devices is a plus.  
• Minimum of 2 years of leading a technical oriented team. 
• Strong practical engineering background in electronic hardware and embedded design for commercial production. 
• Familiar with electronic simulation and design methodologies and tools (e.g., Spice, Altium, VHDL, etc.)
• Familiar with digital communication buses and protocols (e.g., I2C, SPI, UART etc.). 
• Familiar with analog design, preferably implant analog design.  
• Ability to manage projects mandated to external sub-contractors and manufacturing.
• Strong hands-on skills, experience with machine shop tools.
• Fluency in English required (English is company language). 
• Fun, loving, people person. Fast learner, self-motivated and pro-active individual able to work in the fast-moving environment of a dynamic start-up company.
• A system-thinking attitude.
• Team oriented, a sparring partner to colleagues in other disciplines.

• Fluency in Spanish is a plus.
• Preferred to have solid experience in neuroscience with a strong interest in gaining a further understanding of this field.
• Preferred to have experience in applying quality control for medical devices (ISO13485) or in a similar working environment in a tightly regulated industry (e.g., medical devices).
• Preferred to have a solid understanding of Medical Risk Analysis.
• Preferred to have detailed understanding of active implantable medical device development and application of its relevant standards.

• A collaborative 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. You'll 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. You'll 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

• Assemble electronic systems that are part of an implantable neurostimulation system.
• Support in the bring-up and debugging of electronic systems using e.g. oscilloscope, logic analyzer, etc. 
• Develop and assemble (automated) test systems for the characterization and verification of medical electronic systems.
• Support in the verification test execution of electronic subsystems (functional, electrical safety, EMC, reliability).
• Work with external partners in the outsourced design, assembly and test of electronic systems and test systems.
• Provide electronics services to the various project teams.
• Lab management, including equipment quality control, tools maintenance, incoming inspection, etc.
• Work according to quality management system (QMS) and accurately document test results, assembly procedures, change control, traceability, etc.

• Degree in electronics, mechatronics or other relevant education.
• At least 3 years of work experience in a relevant electronics development environment.
• Strong hands-on skills in assembly, bring-up and debugging of electronics systems.
• Experienced in test tool and test system development and assembly.
• Design tools for electronics design and layout.
• Proficient at soldering and reworking components on PCBs.
• Experience working according to assembly SOPs and interpret assembly drawings and schematics.
• Background in lab management activities and responsibilities, e.g. equipment control, tools maintenance, incoming inspections.
• Fluency in English required (English is company language). 
• Fast learner, self-motivated and pro-active individual able to work in the fast-moving environment of a dynamic start-up company.
• Be a team player and Communicate effectively.

• Altium electronics design and layout experience.
• Experience in testing electrical safety according to IEC60601.
• Familiar with electronics manufacturing processes.
• Automated test scripting and execution.

• A collaborative 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. You'll 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. You'll 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

• End-responsible for making decisions on architecture and implementation strategies and guiding the team in all of that.
• Maintains close collaboration and interaction with the systems and product teams.
• Responsible for the delivery, correctness of the documentation stack per embedded subsystem. 
• Responsible for the quality in broadest sense, code quality, testability.
• Ensuring compliance with IEC62304.
• Establish software development best practices, including modular design, coding guidelines, and architectural patterns.

• Bachelor's or Master's degree in a relevant engineering discipline.
• 8+ years of experience in embedded software development, with at least a number of years in architecture/leadership roles.
• Expert in C, with deep knowledge of low-level programming, memory management, and performance optimization.
• Knowledge of embedded debugging techniques (JTAG/SWD, oscilloscopes, logic analyzers, tracing tools).
• Experience with real-time operating systems (RTOS), bare-metal, and Linux-based embedded systems.
• Solid understanding of testing methodologies (unit testing, integration testing, HIL testing, automated test frameworks).
• Demonstrated experience with IEC 62304 and development of software within Medical industry.
• Knowledge of system-level safety and risk management (e.g., ISO 14971, FMEA, fault-tolerant design).
• Experience with CI/CD pipelines for embedded development, version control (Git), and build systems.
• Familiarity with design for manufacturing (DFM) and design for testing (DFT) principles.
• Strong communication skills, with the ability to lead cross-functional discussions and present architecture decisions.
• Able to catch complex system behavior into simple drawings.

• Familiar with Python scripting
• Experience with nightly integration testing on real devices
• Knowledge of cyber security

• A collaborative 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. You'll 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. You'll 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

• Test Strategy & Equipment Setup: Define and deploy the test infrastructure required to characterize 3D MEMS process steps thermal bonding, wafer-level packaging, TGV, electrochemical or mechanical reliability testing. Specify, qualify and operate metrology, electrical test, and reliability equipment.
• Process Characterization & DOEs: Design and execute structured experiments to characterize 3D MEMS unit processes and integrated flows. Generate the data needed to set process windows, control limits, and acceptance criteria across coupled process steps. 
• Data Analysis & Industrialization: Build Python-based data pipelines to analyze high-volume process and test data. Extract yield, Cpk, drift, and failure-mode signatures. Translate findings directly into process and test recipe improvements. 
• Hardware & Electrical Characterization: Lead electrical and physical characterization across 3D MEMS structures. Use SMUs, DAQs, oscilloscopes, probe stations, and dedicated MEMS test rigs to measure critical parameters at the required precision. 
• Materials & Failure Analysis: Apply materials science fluency, thin films, interfaces, integration physics, to root-cause analysis on failures across, bonding, packaging, TGV interfaces and electromechanical reliability. Feed findings back to process and design teams to drive iterations. 
• Cross-Functional Coordination: Work directly with Process Integration, Packaging, Hardware, mechanical and Software teams to align test requirements, hardware specifications, and data infrastructure. Translate 3D MEMS physics into testable specifications across disciplines. 
• Industrialization & Scaling: Take prototype test setups out of R&D and harden them for pilot and production. Author SOPs, qualify equipment (IQ / OQ / PQ), and integrate with MES where applicable. 
• Continuous Improvement: Identify opportunities to reduce variation, improve test throughput, and tighten the link between process control and electrical / yield outcomes across the 3D MEMS stack.
  
  

• Bachelor’s or Master’s degree in Electrical Engineering, Applied Physics, Materials Science, Microelectronics, or a related field. 
• 5+ years in Test Development, Device Characterization, or Yield Engineering within a semiconductor, MEMS, or advanced packaging environment. 
• Vertical Integration & MEMS Expertise: Hands-on experience with testing and characterizing advanced packaging architectures, including wafer-level thermal bonding, Through-Glass Vias (TGV) / TSV metallization, and electromechanical reliability. 
• Data Science & Scripting: High proficiency in Python (e.g., Pandas, NumPy, SciPy) for complex data analysis, instrument control (SCPI/VISA), and automating high-volume, lot-level data workflows.
• Test Equipment & Instrumentation: Hands-on expertise building test setups with SMUs, DAQs, oscilloscopes, and automated metrology tools. Highly capable of debugging signal integrity for low-noise/high-impedance analog measurements. 
• Physics of Failure: Deep understanding of semiconductor/MEMS device physics, thin films, and electromechanical integration. Must understand why an interface fails (e.g., CTE mismatch, delamination, voiding) to design accurate test traps. 
• Industrialization Track Record: Proven ability to take prototype test platforms out of R&D and industrialize them for pilot or production use, including authoring SOPs and executing equipment qualification (IQ/OQ/PQ). 
• Systematic, first-principles approach to problem-solving. 
•  A strong instinct for identifying R&D fragility.
• Strong written and verbal communication.
• Takes full ownership of test strategy, equipment readiness, and data quality. 
• Thrives in fast-moving, unstructured deep-tech environments.

• Database Architecture: Experience interfacing automated test hardware with Manufacturing Execution Systems (MES) or SQL databases, and building visual dashboards (e.g., Grafana, PowerBI) for tracking yield and Cpk.
• Reliability & Environmental Testing: Practical knowledge of accelerated aging models, hermeticity testing (leak rate analysis), and Electrochemical Impedance Spectroscopy (EIS).
• Neurotechnology & Mixed-Signal Electronics: Familiarity with high-channel-count analog front-ends (AFEs), custom ASICs, or complex neural electrophysiology signal chains. 
• Statistical Process Control: Working knowledge of PFMEA, DOE methodology, SPC, and Cpk-driven process control in regulated manufacturing environments. 
• Pilot-to-Production Scaling: Prior experience supporting a deep-tech hardware company through a pilot-to-production transition, including capital tooling and scale-up decisions.

WHAT CAN WE OFFER TO YOU? 

• A collaborative 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. You'll 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. You'll 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
• While we offer flexible working modality, because of the nature of this position, this will be an office-based position in Bellaterra.

• Lead the design, assembly, prototyping and of the mechanical components that are part of an  implantable system in direct collaboration with the electronics, systems, quality and regulatory teams. 
• Design for reliability, manufacture and test, including concept engineering, functional analysis, FEM analysis, and mechanical modelling. 
• Deliver detailed documentation of the device design (BOM, drawings, Specifications, test plan,…) compliant with ISO 13485 and ISO14971 design control requirements.  
• Support and collaborate with external partners in the outsourced design, assembly and test of mechanical components that are part of an implantable VNS system 
• Define test plans and methods to verify safety and mechanical performance of the device, in compliance with applicable standards and in collaboration with other teams.
• Design and build and perform, experimental and product system setups necessary to perform bench tests, characterization testing, integration, system testing. 
• Create test plans to verify our mechanical designs from the product requirements.   
• Initiate and contribute to design, technical and milestone reviews. 
• Understand DFR/DFM/DFT (Design for Reliability, Design for Manufacturing and Design for Test), including concept engineering, modelling, analysis, sensitivity, and stress analysis.  
• Work intensively with Quality, Regulatory, Clinical and Project Management on the formal product development procedure, perform or collaborate in design and stage reviews. 

• BS or MS in Mechanical Engineering with at least 5 years of work experience in Med Tech with a proven experience executing a full development cycle.
• +5 Year experience in the areas required to perform this job: Mechanical CAD design, Selection of medical-grade materials and components, safety and performance testing, Requirements based Design.
• Capable and experience to oversee subcontracted activities.
• Strong hands-on skills, experience with workshop tools.
• Experience in (MDR) Medical Device Regulation, ISO 13485 Quality environments, ISO 14971 Risk Analysis and IEC 60601.
• Fun, loving, people person.  
• Fast learner, self-motivated and pro-active individual able to work in the fast-moving environment of a dynamic start-up company. 
• A system-thinking attitude identify areas of potential improvement and develop plans to address these; Team oriented, a sparring partner to colleagues in other disciplines.

• Preferred to have solid experience in neuroscience with a strong interest in gaining a further understanding of this field. 
• Preferred to have experience in applying quality control for medical devices (ISO13485) or in a similar working environment in a tightly regulated industry (e.g. medical devices); 
• Preferred to have solid understanding of Medical Risk Analysis. 

• A collaborative 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. You'll 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. You'll 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

• Development of medical device electronics that are part of an implantable system, in close collaboration with the mechanical and software teams.
• Translate system requirements and user needs into subsystem and interface requirements.
• Perform functional analysis and create system designs that meet the requirements.
• Manage external partners in the outsourced design, assembly,verificationand validation of electronic systems that are part of the implantable neurostimulation system.
• Support the system integration and process development.
• Define test strategies to verify the electronics and system against the product requirements and applicable standards for electrical safety,  EM and MRI compatibility.
• Apply risk management and perform design failure mode and effect analysis (DFMEA) on designs.
• Initiate and lead design reviews, technical reviews, and milestone reviews.
• Lead and participate in system integration, verification, and validation.
• Understand and apply DFR/DFM/DFT (Design for Reliability, Design for Manufacturing and Design for Test), including concept engineering, modelling and statistical analysis.

• BSc or MSc in Electronics Engineering.
• At least 6 years of work experience in a relevant medical device development environment.
• Experienced in the full development cycle of a medical device including design, manufacturing, verification, and validation.
• Experienced in the development of wireless power transfer systems and applicable regulations.
• A system-thinking attitude, identify areas of potential improvement and develop plans to address these; Team oriented, a sparring partner to colleagues in other disciplines.
• Experienced with electronic simulation and design methodologies and tools (e.g., Spice, Altium, etc.) and PCB design according to IPC standards.
• Experienced in Verification test design and execution including statistical analysis.
• Solid understanding of Medical Risk Analysis and FMEA.
• Experienced in managing development outsourced to subcontractors for design, manufacturing, and integration.
• Solid understanding of medical device development standards and experience in applying these standards (IEC-60601-1, IEC-60601-2) in medical device electronics design and verification.
• Fluency in English required (English is company language).
• Determination to develop yourself.
• Be a team player.
• Communicate effectively.
• Think and act strategically.

• Experience with active medical implantable devices and the ISO 14708standard. 
• Experience in neuroscience.

• A collaborative 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. You'll 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. You'll 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