SOFTWARE ENGINEERING

Position Overview

We are seeking an experienced Software Engineering to play a key role in the development of scalable, compliant, and cutting-edge MedTech solutions deployed in the cloud. In this role, you will focus primarily on hands-on software development, contributing to the design, architecture, and implementation of critical software components while ensuring best practices and technical excellence throughout the development lifecycle.

You will join an extremely motivated team committed to performing high-impact work in the precision medicine field, collaborating closely with cross-functional teams, including product management, data science, quality assurance, and regulatory affairs, to align software solutions with business and healthcare regulatory objectives.

EU citizens will be requested a registration certificate in Spain. Non-EU residents must hold a valid residence and work permit. Additionally, all applicants must possess educational qualifications that are accredited or recognized by the Ministry of Education to ensure compliance with the standard educational requirements for the role.

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Key Responsibilities

• Software Development: Design, develop, and implement scalable software solutions with clean and efficient code.
• Technical Problem-Solving: Analyze technical challenges and propose innovative solutions to meet performance, scalability, and security requirements.
• Quality Assurance: Write and maintain unit and integration tests to ensure software reliability and compliance with ISO quality management standards.
• Cross-functional Collaboration: Work closely with product managers, data science, quality assurance, and regulatory affairs teams to align engineering efforts with business and regulatory goals. Ensure seamless communication and collaboration between departments to drive project success.
• Deliverability & Quality Assurance: Take full ownership of project deliverables, ensuring that all software releases meet FDA and CE compliance requirements, are tested rigorously, and adhere to ISO quality management system standards. Collaborate with QA to establish and maintain automated testing pipelines for faster and more reliable releases.

• Process Improvement & Best Practices: Define and implement best practices for agile development, code reviews, continuous integration/continuous delivery (CI/CD) pipelines, and DevOps practices. Strive for continual improvement in the team’s software development processes.

• Technical Guidance & Innovation: Ensure software design and architecture meet the performance, scalability, and compliance requirements. Stay updated on emerging technologies and industry trends, especially related to cloud computing, machine learning and data security in healthcare.

• Regulatory Compliance: Ensure all software development efforts are aligned with FDA, ISO, GDPR, and other relevant regulatory standards. Collaborate with the regulatory affairs team to support submission processes and audits.

Qualifications & Skills:

Education:

Bachelor’s or Master’s degree in Computer Science, Software Engineering, or a related field.

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Experience:

• 5+ years of experience in software engineering, ideally in a regulate environment such as MedTech or healthcare.
• Hands-on experience with cloud platforms (AWS, Azure, GCP) and microservices architecture.
• Familiarity with FDA & ISO and other relevant healthcare standards.
 

Technical skills:

• Experience with modern software development languages and frameworks, such as Python, Java, C++, or JavaScript.
• Expertise in agile methodologies, CI/CD pipelines, and automated testing.
• Solid understanding of software security best practices,especially in handling sensitive medical data (HIPAA, GDPR).

Soft skills:

• Strong problem-solving skills and the ability to troubleshoot complex technical issues.
• Excellent communication and teamwork abilities in cross-functional settings.
• Ability to adapt to a fast-paced, evolving environment while maintaining high attention to detail.
  

 Languages:

English and Spanish

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Nice to Have:

• Experience in developing AI-driven or SaMD (Software as a Medical Device) solutions.

• Experience in project management and team leadership.
 
• Certifications such as Certified ScrumMaster (CSM), PMP, or equivalent.
 
• Knowledge/understanding of applicable FDA regulations to IVD, the IVDR, GDPR, ISO 13485, ISO 62304

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Application Documents

• Curriculum Vitae (including your contact details)
• Motivation Letter

Posting Contact Information

Candidates must submit the documents via email: info@reveal-genomics.com, including the reference code Ref. 01-2025.

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General Data Protection Regulation

Pursuant to current legislation on Data Protection, specifically, Regulation (EU) 2016/679 and Organic Law 3/2018 PDGDD, we inform you that the personal data you will voluntarily provide us with through your CV, forms, tests and face-to-face interviews will become part of our information systems, owned by REVEAL GENOMICS, S. L. and will only be processed to manage your application in this selection process or in subsequent processes compatible with your professional profile, processing to which you expressly consent by signing this document.

If you are not a selected candidate, the data provided will be kept for a maximum period of 2years from the end of this selection process. These data will not be passed on or communicated to third parties, except in the case of legal obligation.

 You have the right to obtain confirmation as to whether or not we are processing your personal data and you, therefore, have the right to access your personal data, rectify inaccurate data, or request their erasure when the data are no longer necessary, by writing to C.Villarroel, 170 2º 5ª, 08036 Barcelona or via email to: info@reveal-genomics.com  You can contact the competent supervisory authority (www.aepd.es) for any complaint you may have.

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