Ofertes d'ocupació a GE Healthcare

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Job Description Summary

We are looking for a Regulatory Affairs Intern to support medical device registration in Iberia, while working in a global environment and collabortating with manufacturing sited. This is a strategic project arising from Royal Decree 192/2023 and EU Regulation 2024/1860, which require the registration of all medical devices in the AEMPS (RECOPS) database, integrated with EUDAMED.

This role is an excellent opportunity for someone seeking to start a career in Medical Device Regulatory Affairs within a technical, multicultural, and highly collaborative environment.

GE Healthcare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world

GE HealthCare ha sido reconocida como una de las 100 Mejores Empresas para Trabajar en España en 2025, según el ranking de Actualidad Económica–El Mundo.

Responsibilities

Job Description

• Support the registration of medical devices in the RECOPS database.
• Prepare, review, and upload technical documentation ensuring alignment with EUDAMED.
• Identify additional products requiring registration (OEM devices, accessories, variations).
• Assist with fee management through internal corporate workflows.
• Maintain master lists and support project tracking activities.
• Collaborate with internal teams (Quality, Logistics, Marketing, Product Managers).
• Provide regulatory support to Sales and Technical Service teams.
• Contribute to project reports, progress updates, and audit preparation.
  
  

• Final-year student or recent graduate in: Health Sciences, Engineering, Bioengineering, Chemistry, Physics, Pharmacy, or related scientific fields.
• Ability to manage and provide a training/internship agreement with a university (or equivalent), enabling a scholarship/internship program with an estimated duration of 12 months.
• Fluency in English and Spanish (spoken and written).
  
  

• Postgraduate degree in Regulatory Affairs or specialized training in medical device regulation (MDR/IVDR), quality, or regulatory compliance.
• Portuguese and other EU languages are a plus.
• Strong interest in medical device regulation and EU regulatory frameworks.
• Ability to work with detailed technical information.
• Ability to work independently in fast-paced environment with little supervision
• Solid knowledge of Excel and digital tools.
• Excellent organization, accuracy, and written communication skills.