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