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.

Job Description

Responsibilities

• 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.

Qualifications and Requirements

• 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).

Desired Characteristics

• 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.

Inclusion and Diversity:

GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Behaviours:

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

Total Rewards:

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration, and support.

#LI-Hybrid

#LI-AV1

Additional Information