Medical Device Software Engineer - Regulated, Cloud

Sci-Rec

Barcelona

Presencial

EUR 40.000 - 70.000

Jornada completa

14 días+

Recibe más respuestas de empleadores

Envía un currículum específico para el puesto de trabajo en cuestión de minutos.

Descripción de la vacante

Sci-Rec in Spain is seeking a Software Engineer to support regulated medical device software and digital infrastructure. You will work across the full development lifecycle, collaborating with hardware, data, regulatory and quality teams to deliver reliable, secure and compliant medical applications.

The role focuses on architecture, cloud infrastructure, verification, and the preparation of technical documentation required within a regulated medical device environment.

Formación

  • Degree in Computer Science, Computer Engineering, Telecommunications Engineering or related field.
  • At least two years’ experience in software development and testing, ideally within a medical device or similarly regulated environment.
  • Strong programming knowledge across C#, .NET, C++, MATLAB or comparable technologies.
  • Practical knowledge of Git-based version control and software release processes.
  • Experience building cloud infrastructure using AWS or a similar platform.
  • Understanding of software verification, validation and traceability.
  • Knowledge of IEC 62304, EU MDR, MDCG guidance and FDA requirements.
  • Understanding of cybersecurity and data-protection frameworks, including GDPR, NIS2 and HIPAA.

Responsabilidades

  • Develop, test and maintain medical device software across the full development lifecycle.
  • Contribute to software architecture and communication between user interfaces, backend systems and algorithmic modules.
  • Develop well-designed and efficient software using technologies including C#, .NET, C++, MATLAB and WPF/XAML.
  • Support the integration of signal-processing, algorithmic and MATLAB-derived modules.
  • Build and maintain cloud infrastructure using AWS or similar platforms.
  • Conduct unit, integration, regression and software verification testing.
  • Support automated testing, static code analysis, code coverage and CI/CD processes.
  • Prepare test protocols, datasets, expected results and verification records.
  • Maintain traceability between requirements, risks, design, code, tests, defects and software releases.
  • Investigate and resolve software defects and verification deviations.
  • Maintain Git repositories, branching strategies, pull requests, tags, releases and code review workflows.
  • Prepare and maintain software lifecycle and technical documentation, including architecture, design, traceability, risk management and verification records.
  • Support software cybersecurity and data-protection activities.
  • Analyse system performance, including sensitivity, specificity and output consistency.
  • Coordinate software changes, technical impact assessments and controlled releases.
  • Collaborate with external software development or testing providers where required.
  • Ensure development activities comply with applicable quality and regulatory requirements.

Conocimientos

C#
.NET
C++
MATLAB
WPF/XAML
Git

Educación

B.S./B.Eng. in CS/CE/Telecom or related

Herramientas

AWS

Descripción del empleo

Sci-Rec in Spain is seeking a Software Engineer to support regulated medical device software and digital infrastructure. You will work across the full development lifecycle, collaborating with hardware, data, regulatory and quality teams to deliver reliable, secure and compliant medical applications.

The role focuses on architecture, cloud infrastructure, verification, and the preparation of technical documentation required within a regulated medical device environment.

Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra y suelta tu archivo aquí
Similar jobs

Puestos de trabajo similares que vale la pena comparar

Software Engineer
Software Engineer

Sci-Rec • Barcelona

Presencial
EUR 40.000 - 70.000
Systems Engineer - (Medical industry)
Systems Engineer - (Medical industry)

Global Life Science Hub • Barcelona

Presencial
EUR 50.000 - 70.000
Remote Senior Quality & Regulatory Lead - Medical Devices
Remote Senior Quality & Regulatory Lead - Medical Devices

Sener Diagnostics • Barcelona

Presencial
EUR 90.000 - 130.000
International projects
Flexible working hours & remote work
Flexible remuneration plan
+4
Lead Embedded Software Engineer - Hybrid Medical Devices
Lead Embedded Software Engineer - Hybrid Medical Devices

D.med Software • Málaga

Híbrido
EUR 90.000 - 120.000
Private health insurance
Team events
Benefits at work access
Senior Regulatory Affairs: Medical Devices & AI Software
Senior Regulatory Affairs: Medical Devices & AI Software

ClarkeModet • País Vasco

Híbrido
EUR 70.000 - 90.000
Hybrid work
International projects
Professional growth
Hybrid Embedded Firmware Engineer — Medical Devices
Hybrid Embedded Firmware Engineer — Medical Devices

D.med Software • Málaga

Híbrido
EUR 45.000 - 64.000
Private health insurance
Benefits at work
Team events
+1
Senior Regulatory & Quality Lead — Medical Devices (Hybrid)
Senior Regulatory & Quality Lead — Medical Devices (Hybrid)

Sener en Ingeniería • Cerdanyola del Vallés

Presencial
EUR 90.000 - 130.000
International projects
Flexible working hours and remote work
Private medical insurance
+4
Regulatory Affairs Specialist
Regulatory Affairs Specialist

Rob Surgical • Barcelona

Presencial
EUR 65.000 - 90.000
Competitive salary
International and multidisciplinary R&
Senior Software Engineer Technical Lead
Senior Software Engineer Technical Lead

D.med Software • Málaga

Híbrido
EUR 90.000 - 120.000
Private health insurance
Team events
Benefits at work access
Global QMS Systems Engineer: Digital Quality & Compliance
Global QMS Systems Engineer: Digital Quality & Compliance

Align Technology • Madrid

Presencial
EUR 45.000 - 65.000