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Regulatory Affairs Intern

On-site in Sant Boi de Llobregat·Added 5 days ago

Overview

Requirements

  • Have the right to work in Spain

    Synthon Hispania doesn't mention sponsorship in the ad.

  • Work in English

    English is required, per the ad.

  • Work on-site in Sant Boi de Llobregat

    No relocation package mentioned.

  • Master's degree

    “Estudiante del Master en Industria Farmacéutica y Parafarmacia o del Master en Registro Farmacéuticos y Productos Afines.” — per the ad.

This job was automatically translated to English.

Pay & benefits

What you'll get

  • Be part of a dynamic work environment based on trust and transparency.
  • Schedule: to be agreed with the selected candidate (6h-8h/day preferably between 8:00 and 16:00).
  • Start date: October 01, 2026
  • Internship Agreement

Requirements

What we're looking for

  • Student of the Master's in Pharmaceutical Industry and Parapharmacy or the Master's in Pharmaceutical Registration and Related Products.
  • Advanced level of English (speaking/writing essential).
  • We are looking for responsible, motivated people with the ability to work in a team.

The role

Reporting to the Regulatory Affairs Department Manager, the Regulatory Affairs Intern will be assigned the following support functions for the department:

What you'll do

  • Preparation of AI/IB variation documentation, revalidations, deficiency letters, Transfers, CPPs, etc.
  • Submission of the registration dossier: collect all necessary additional information from Module 1 of the Registration dossier (specific national requirements and client requirements) and provide support for the dossier submission.
  • Preparation of Documentation - Module 3.
  • Enter and maintain the applicable databases of the department
  • Final preparation of national phases. Translation/Review of Summary of Product Characteristics, package leaflet, labeling (AEMPS splitting platform)

About Synthon Hispania

Synthon is a leading international pharmaceutical company specialized in the development, manufacturing and commercialization of complex generic pharmaceuticals globally.

Its Spanish entity, Synthon Hispania, contributes to Synthon's mission by developing, producing and coordinating the supply of affordable, high-quality generic pharmaceutical products, and the Spain site is focused on Research and Development and Drug Product Manufacturing. Current openings at Synthon Hispania include QA and QC technician and analyst roles, R&D project management, pharmaceutical technology and regulatory affairs internships, and applications/IT positions, indicating an operationally and scientifically oriented site relevant to pharmaceutical professionals in Spain.

Industry
Pharmaceuticals
Founded
1991

Good to know if you are moving

  • The Spain site is focused on Research and Development and Drug Product Manufacturing within Synthon's global network.
  • Synthon Hispania develops, produces and coordinates supply of affordable, high-quality generic pharmaceutical products for Synthon's customers.
  • Current Spain openings include QA and QC roles, Project Manager R&D, Applications Technician and intern (becario/a) positions in Pharmaceutical Technology and Regulatory Affairs.
All open roles at Synthon Hispania
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