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Medical Device AI Software Quality Engineer

SQS-Software Quality Systems, S.A

España

Presencial

EUR 30.000 - 45.000

Jornada completa

Hoy
Sé de los primeros/as/es en solicitar esta vacante

Descripción de la vacante

A technology company in Spain seeks a Medical Device AI Software Quality Engineer. The role involves developing validation strategies for medical devices, preparing test documentation, and ensuring compliance with regulatory standards. Ideal candidates will have a background in mathematics, physics, or engineering, and be proficient in English and Spanish. This is an entry-level full-time position with opportunities for professional growth in a dynamic environment.

Servicios

Work in interesting projects
Continuous learning
Professional growth opportunities
Collaborative environment

Formación

  • Proficiency in English and Spanish.
  • Experience in preparing technical documentation.
  • Familiarity with front-end and back-end software technologies.

Responsabilidades

  • Develop validation and verification strategies for medical devices.
  • Prepare and execute test plans.
  • Provide consulting on software development processes.

Conocimientos

Knowledge of artificial intelligence applied to medical devices
Ability to work autonomously
Public speaking skills

Herramientas

ISO 13485
IEC 62304
GMP
Descripción del empleo
Medical Device AI Software Quality Engineer

At SQS, we are looking for mathematicians, physicists, biomedical, computer scientists, or telecommunications engineers with proficiency in both English and Spanish and an interest in developing in the field of medical software quality that incorporates artificial intelligence. The position is to join our office in Rivas-Vaciamadrid within the health area team (medical devices and pharmaceutical laboratories).

Responsibilities
  • Develop validation and verification strategies for both medical devices and software equipment used in pharmaceutical manufacturing laboratories
  • Prepare test plans
  • Execute test plans
  • Prepare technical documentation required for the technical file
  • Provide consulting on software development processes
  • Write technical articles, give presentations, and conduct training sessions
  • Stay up-to-date with regulatory aspects
Qualifications
  • Knowledge of artificial intelligence applied to medical devices
  • Experience in preparing technical documentation
  • Experience in software development and testing
  • Familiarity with front-end and back-end software technologies, as well as development tools
  • Ability to work autonomously
  • Public speaking skills
  • Knowledge of standards such as : ISO 13485, IEC 62304, and GMP
  • Regulatory knowledge of FDA, EU MDR, AI, and GMP

Join a growing team and work in a highly dynamic and innovative environment!

We offer
  • Work in interesting projects
  • Continuous learning
  • Professional growth opportunities
  • Working in a collaborative environment

If you enjoy continuous learning, challenges, technology, and the application of artificial intelligence to the health sector, this is your challenge!

Seniority level

Entry level

Employment type

Full-time

Job function

Engineering and Information Technology

Industries

IT Services and IT Consulting

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