Software Engineer

Sci-Rec; Barcelona; Presencial; EUR 40.000 - 70.000; Jornada completa

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

wAn innovative medical technology company is seeking a Software Engineer to support the development and continuous improvement of regulated medical device software and associated digital infrastructure

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Reporting directly to the CTO, this individual will contribute across the full software lifecycle, working closely with hardware, data, regulatory and quality teams to deliver reliable, secure and compliant medical application

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The R

oleThe Software Engineer will be responsible for gathering requirements, defining system functionality and developing high-quality, testable software. The role will also support software architecture, cloud infrastructure, verification, cybersecurity testing and the preparation of technical documentation required within a regulated medical device environme

nt.
Key Responsibili

• tiesDevelop, test and maintain medical device software across the full development lifecy
• cle.Contribute to software architecture and communication between user interfaces, backend systems and algorithmic modu
• les.Develop well-designed and efficient software using technologies including C#, .NET, C++, MATLAB and WPF/X
• AML.Support the integration of signal-processing, algorithmic and MATLAB-derived modu
• les.Build and maintain cloud infrastructure using AWS or similar platfo
• rms.Conduct unit, integration, regression and software verification test
• ing.Support automated testing, static code analysis, code coverage and CI/CD proces
• ses.Prepare test protocols, datasets, expected results and verification repo
• rts.Maintain traceability between requirements, risks, design, code, tests, defects and software relea
• ses.Investigate and resolve software defects and verification deviati
• ons.Maintain Git repositories, branching strategies, pull requests, tags, releases and code review workfl
• ows.Prepare and maintain software lifecycle and technical documentation, including architecture, design, traceability, risk management and verification reco
• rds.Support software cybersecurity and data-protection activit
• ies.Analyse system performance, including sensitivity, specificity and output consiste
• ncy.Coordinate software changes, technical impact assessments and controlled relea
• ses.Collaborate with external software development or testing providers where requi
• red.Ensure development activities comply with applicable quality and regulatory requireme

nts.
Candidate Pr

• ofileDegree in Computer Science, Computer Engineering, Telecommunications Engineering or a related technical discip
• line.At least two years’ experience in software development and testing, ideally within a medical device or similarly regulated environ
• ment.Strong programming knowledge across C#, .NET, C++, MATLAB or comparable technolo
• XAML.Practical knowledge of Git-based version control and software release proce
• sses.Experience building cloud infrastructure using AWS or a similar plat
• form.Understanding of software verification, validation and traceabi
• lity.Knowledge of regulated software standards such as IEC 62304, EU MDR, MDCG guidance and FDA requirem
• ents.Understanding of cybersecurity and data-protection frameworks, including GDPR, NIS2 and H
• IPAA.Embedded software experience would be advantag