Senior Software Engineer

Neuroelectrics is a creative, high-tech company offering the best-in-class non-invasive and high-definition electrical brain stimulation technology for personalized neuromodulation. By measuring and modifying brain function, we aim to restore brain health, minimize disabilities and create a better life for patients.
We are looking for new members of our team who already live by our shared values and are inspired by our company's Vision. Accelerate the evolution of brain science and technology by delivering advanced solutions to help end patients suffering from brain pathologies; and our Mission. Revolutionize the understanding of the brain through new personalized neuromodulation therapies, anywhere and at any time.

We need a Senior Medical Device Software Engineer with a strong background in software development, technical documentation, and quality assurance processes. The ideal candidate will possess in-depth knowledge of software requirements and design specification, software risk analysis, and expertise in designing comprehensive verification and validation tests.

• Develop and maintain software for neuromodulation and EEG devices, ensuring performance, safety, and commpliance with medical device standards and regulations.
• Author high-quality technical documentation, including software requirements specifications (SRS), software design specifications (SDS), and test protocols.
• Conduct software risk analysis to identify potential issues and develop mitigation strategies, ensuring patient safety and device effectiveness.
• Review verification and validation tests for software functionalities, ensuring compliance with both internal standards and external regulatory requirements.
• Collaborate with cross-functional teams, including product owners, hardware engineers, clinical researchers, and regulatory affairs, to ensure cohesive development and documentation efforts.
• Stay abreast of industry trends, regulatory changes, and advancements in technology to continually improve our software development and documentation practices.
• Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering, or a related field. A Master's degree is preferred.
• Minimum of 4 years of experience in software development for medical devices, with a strong portfolio demonstrating expertise in technical documentation and quality assurance.
• Expertise in C/C++ and Python. Knowledge of GUI programming for Desktop applications.
• Knowledge about the development of desktop applications with GUI using C++, C#, Java or others.
• Familiarity with the Qt framework.
• Knowledge of cloud/web technologies (Azure/AWS, SQL Server, REST, Flask...).
• Working knowledge of Matlab.
• Notions of FPGA programming.
• Knowledge of regulatory standards applicable to medical device software development, such as IEC 62304, ISO 14971, FDA guidelines, and European regulations (MDD, MDR, etc.).
• Demonstrated experience with software requirements specification (SRS), software design specifications (SDS), software risk analysis, and the creation of verification and validation tests.
• Excellent analytical, problem-solving, and communication skills, with the ability to explain complex technical concepts to non-technical stakeholders.
• Familiarity with modern software development tools, languages, and methodologies.
• Strong attention to detail and commitment to delivering high-quality, compliant software solutions.
• Passionate about making a difference, gifted with a can-do attitude.
• Reliable, Responsible, and Respectful.
• Good communication and presentation skills.
• Ability to adapt and work effectively within a rapidly changing and growing environment
• Entrepreneurial spirit with the hunger to succeed; act with a founder’s mindset: have urgency, and grit, be adaptable to change, and push boundaries
• Team player, collaborative, innovative, get things done mind
• Show initiative in setting and meeting goals within an environment of managed change
• Ability to work under pressure, responsible for multiple vital tasks in parallel
• Commitment to quality.
• Competitive salary in the sector (according to your experience/skills)
• 26 vacation days per year + 24th and 31th of December
• Fully stocked kitchen (Coffee, organic fruits, snacks, and beverages)
• Flexible Working Hours
• Short Fridays
• Hybrid work
• Private Health insurance, including dental coverage.
• Professional development and collaborative environment
• Unique opportunity to join our company early with excellent market traction and huge potential to grow
• Incredible office in Barcelona in Av. Tibidabo. (shower, stunning views of all of Barcelona, etc.)
• Team Building Events
• Much more still to come