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Trainee (Pharmaceutical Manufacturing and Inspections under the New EU Legislation)

AmsterdamEUR2K - EUR2K / monthPosted 1 weeks ago
Internshiphybridintern

Job Description

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 Inspections Office.

Specific objectives and projects

Context

The EU has launched the most profound and ambitious revision of pharmaceutical legislation in the last 20 years. The Agency, together with the EU regulatory network, is preparing to implement new requirements concerning manufacturing, such as decentralised manufacturing, the Joint Audit Programme (JAP) for Good Distribution Practice (GDP), and enhanced oversight of medicines manufacturing.
 
Project tasks
 
Contribute to the development of new processes and procedures related to the implementation of the new pharmaceutical framework in the area of manufacturing and inspections.
 
Contribute to activities related to the implementation of new regulatory requirements and associated change management processes.
 
Participate in discussions with inspectors, assessors and other stakeholders within the EU regulatory network.
 
Contribute to the preparation of briefing documents and presentations related to the implementation of the new legislation.

Learning outcomes

Through this project, the trainee will:
 
develop knowledge of the regulatory framework for pharmaceutical manufacturing and inspections, as well as EU regulatory network processes;
 
gain experience working on multidisciplinary regulatory projects;
 
gain insight into how EMA collaborates with the EU regulatory network and stakeholders in the context of manufacturing and inspections.

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;
  • project management/organisational 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

 

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Trainee (Pharmaceutical Manufacturing and Inspections under the New EU Legislation) at European Stability Mechanism | Renata