Java Software Engineer For Telecoms

SISU Group; Comunidad Valenciana; Presencial; EUR 40.000 - 80.000; Jornada completa

Descripción de la vacante

Una empresa innovadora busca un Ingeniero de Sistemas Senior para liderar el desarrollo de productos en el sector de dispositivos médicos. Este rol desafiante implica gestionar el ciclo de vida del producto, desde la concepción hasta la entrega, asegurando que se cumplan todos los requisitos regulatorios y de calidad. El candidato ideal tendrá una sólida formación en ingeniería, experiencia en entornos altamente regulados y un enfoque proactivo para resolver problemas. Ofrecemos un entorno colaborativo donde las ideas innovadoras son bienvenidas y se fomenta el crecimiento profesional. Únete a nosotros para marcar una diferencia significativa en la industria y en la vida de las personas.

Servicios

Seguro de salud privado

Bonificación por formación

23 días de vacaciones al año

Semana de Navidad libre

Flexibilidad horaria

Formación

• Experiencia de al menos 5 años en dispositivos médicos o entornos altamente regulados.
• Capacidad para trabajar en un equipo diverso y dinámico.

Responsabilidades

• Liderar el ciclo de vida del desarrollo del producto y la integración de sistemas.
• Colaborar con equipos de calidad, regulatorio y gestión de proyectos.

Conocimientos

Ingeniería de sistemas

Comunicación efectiva

Pensamiento analítico

Liderazgo

Trabajo en equipo

Inglés fluido

Educación

Grado en ingeniería

Máster en ingeniería

Herramientas

Metodologías ágiles

Automatización de pruebas

Descripción del empleo

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Position : Senior Systems Engineer

Location : Barcelona, Kingdom Of Spain, ES

Main Responsibilities :

• Own the product development lifecycle, including maintenance and service.
• Guide the development team in manufacturing process qualifications and validations.
• Organize technical reviews, contribute to design reviews and milestone reviews.
• Translate customer requirements into system requirements and interface definitions.
• Establish system design and decompose the system into lower-level building blocks.
• Daily review, design, requirements, and integration activities.
• Work with Quality, Regulatory, Clinical, and Project Management on formal product development processes.
• Assess feasibility of technology and contribute to technical concepts.
• Lead system integration and system testing of prototypes.
• Perform functional analysis and create system designs meeting requirements.
• Contribute to high-level technical planning, supplier work package definition.
• Assess applicability of standards and norms.
• Initiate preliminary hazard analysis and establish the risk management plan.
• Lead FMEA (Failure Mode and Effects Analysis) on system level.
• Create master verification plan for product and manufacturing requirements.
• Ensure traceability between requirements, test cases, verification, and reports.
• Create, maintain, and monitor configuration management.
• Generate intellectual property.
• Follow change request processes.

Mandatory Qualifications and Soft skills :

• Bachelor's or Master's degree in a relevant engineering discipline.
• Relevant industry experience of at least 5 years in medical devices or another highly regulated environment.
• Fluent in English oral and written (company language).
• Strong engineering background (e.g., mechanics, electronics, software) with a generalist view of system engineering.
• Experience in delivering systems to clinical trials or the market (preferably active implantable medical devices).
• A system thinking attitude, identify areas of potential improvement and develop plans to address them.
• A high-energy, self-motivated, and pro-active individual able to work in a diverse team in a startup company.
• Good analytical skills.
• Reliable, pragmatic, and result-oriented.
• Good communication and presentation skills.
• Leadership or team management skills.
• Able to facilitate work in a nice and constructive manner with different internal engineering and operational disciplines, as well as external stakeholders.

Nice to have :

• Preferably experience with the development of active implantable medical devices.
• Experience with DRM / DFT (Design for Reliability, Manufacturing, and Test).
• Familiarity with agile processes, continuous development, continuous integration, and test automation.
• Experience in manufacturing process qualifications and validations.

Why us?

We are looking for someone who is ready to proactively bring new ideas to the team, push boundaries, and constantly look for innovation. At INBRAIN we believe in shared success and diverse ways of thinking, here you'll learn, grow, and advance in an innovative culture.

WHAT CAN WE OFFER TO YOU?

• A collaborative environment where innovative ideas flourish and teamwork drives us forward.
• 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.
• Cutting-Edge Technology Exposure : Joining us means immersing yourself in the latest technologies and innovative solutions.
• Competitive salary (according to your experience / skills).
• Payflow & Flexflow.
• Private Health Insurance.
• Training bonus for professional development and access to Udemy platform.
• 23 vacation days per year.
• Christmas week off.
• Hybrid working modality.

Applications must be submitted in English. At INBRAIN, we're not just offering a job – we're inviting you to be part of a transformative journey. Are you ready to transform lives? Join us!

Diverse and inclusive: We believe that a diverse and well-balanced workforce drives innovation. At INBRAIN, we foster the inclusion of all people regardless of culture, age, gender, sexual orientation and identity, or any other status.

About us: Learn more about us at INBRAIN NEUROELECTRONICS.com