INTERNSHIP DETAILS

Trainee (Implementation of the new pharma legislation for marketing authorisations and incentives)

CompanyEMA
LocationAmsterdam
Work ModeOn Site
PostedApril 10, 2026
Internship Information
Core Responsibilities
The trainee will contribute to developing new processes and procedures for implementing the new pharmaceutical framework, focusing on centralized procedures and new regulatory incentives to support innovation. Tasks also include collecting and analyzing regulatory information for knowledge management and training related to the new legislation.
Internship Type
full time
Company Size
1687
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
The European Medicines Agency (EMA) is a decentralised body of the European Union with headquarters in Amsterdam. Its main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary use.
About the Role

Selection procedure reference: EMA/TR/11365 

Deadline for applications: 06 May 2026 23:59 CET 

 

The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU), located in Amsterdam. It began operating in 1995. It is responsible for the scientific evaluation, supervision and safety monitoring of medicines in the EU.

 

This traineeship opportunity is now open for applications until 06 May 2026 23:59 CET, with an intake on 1 October 2026.

About the traineeship programme

The Agency is looking for motivated, qualified recent graduates or students on an Erasmus+ or other programme or PhD students or Master's students (who posses a previous degree), who are interested in gaining experience and contribute to the Agency’s work for every patient in Europe. The purpose of a traineeship at the Agency is to perform tasks that are predominantly in the interest of the trainee’s training and principally serve to increase the trainee’s knowledge and to gain relevant experience.

Placement description

We are looking for a trainee in the Regulatory Affairs Office.

Specific objectives and projects

The EU has launched the most profound and ambitious revision of the pharmaceutical legislation in the last 20 years. The Agency, together with the EU regulatory network, is preparing to implement the new framework, which aims to better regulate innovation and increase the availability and affordability of medicinal products.
 
Project tasks
  • Contribute to the development of new processes and procedures supporting the implementation of the new pharmaceutical framework, in particular improvements to centralised procedures and the development of new regulatory incentives and measures to support innovation.
  • Collect and analyse regulatory information to contribute to regulatory knowledge management and training activities related to the new pharmaceutical legislation.

Learning outcomes

Through this project, the trainee will:
 
  • develop a deep knowledge of the regulatory framework for medicinal products for human use and for medical devices;
  • become familiar with regulatory requirements, Agency processes, and regulatory practices related to medicinal products;
  • gain experience in working on multidisciplinary projects involving regulatory, legal, scientific and stakeholder aspects;
  • gain knowledge of the functioning of EMA within the EU regulatory network (European Commission, national authorities, committees, etc.).

 

Eligibility criteria

To be eligible for consideration for this placement, you are required to:

  1. enjoy full rights as a citizen of a European Union Member State or Iceland, Lichtenstein and Norway;
  2. possess a university degree in pharmacy, medicine or life sciences (minimum of three years or more) that must have been obtained between 6 May 2025 and 6 May 2026 or be a university student on an Erasmus + or a similar programme or a PhD student or a Master's student with a previous fully finished degree in the areas mentioned before.
  3. a thorough knowledge of English (at least level C1) and good knowledge of other official EU language (at least B2) of the Common European Framework for Languages

 

For criteria 1 and 2, you will be required to provide proof in the application form and at the interview stage. Failing to present these documents may result in the disqualification from the procedure.

Additional skills

In addition to the eligibility criteria, you will have:
  • analytical skills
  • communication skills

Behavioural Competencies

You will demonstrate the following behavioural competencies:

  • Communication skills
  • Interpersonal skills
  • Working with others
  • Adaptability
  • Research and analytical skills
  • Learning and development

Conditions of traineeship

The traineeship is offered for 10 months (1 October 2026 – 31 July 2027) and takes place at the Agency’s premises in Amsterdam with possibility for teleworking up to 40% of working time from The Netherlands and occasional teleworking from outside The Netherlands. Traineeships are offered for either full-time or part-time (80% or 50%) if combined with university studies.

The Agency pays a monthly stipend of €2,049.77 for a full-time traineeship (reduced accordingly for 80% or 50%) and a travel contribution upon joining the Agency.

Each trainee will have a mentor at the Agency who will guide the trainee through the programme.

The conditions of employment are stated in the Executive Decision on rules governing the traineeship programme at the EMA available here.

Expected selection timelines

Deadline for applications 06 May 2026 23:59 CET 
Assessments (remote)From mid-June 2026 to mid-July 2026
Decision and offers By end of July 2026
Placement start 1 October 2026

 

______________________________________________________________________________________________________

Domenico Scarlattilaan 6 - 1083 HS Amsterdam - The Netherlands

Telephone +31 (0)88 781 6000 - Email recruitment@ema.europa.eu

 

© European Medicines Agency, 2024. Reproduction is authorised provided the source is acknowledged.

Key Skills
Analytical SkillsCommunication SkillsInterpersonal SkillsAdaptabilityResearchRegulatory AffairsPharmaceutical LegislationProcess DevelopmentKnowledge ManagementTraining Activities
Categories
LegalHealthcareScience & ResearchGovernment & Public Sector
Benefits
Travel Contribution