Regulatory Affair Intern - Medical Device

AbbVie

Sesto San Giovanni, Italy
Not specified
Scientific degree required
Mdr regulation knowledge
Analytical and detail-oriented
AbbVie is seeking a Regulatory Affairs Intern in Sesto San Giovanni, Italy, to assist with the registration of medical devices in Spain and Portugal, focusing on high-risk devices in cardiology and neuromodulation. The role provides an opportunity to gain practical knowledge of regulatory requirements and collaborate with international teams

Job Summary

  • The intern will support the Regulatory Affairs team with medical device registration activities in Spain and Portugal following EUDAMED implementation.
  • This role offers an opportunity to deepen knowledge of regulatory requirements for high-risk devices in cardiology and neuromodulation sectors.
  • Responsibilities include analyzing device registration needs, collaborating with Marketing on priorities, and verifying documentation according to competent authority requirements.

Matching Summary

Match Score: 75

AbbVie is seeking a Regulatory Affairs Intern in Sesto San Giovanni, Italy, to assist with the registration of medical devices in Spain and Portugal, focusing on high-risk devices in cardiology and neuromodulation. The role provides an opportunity to gain practical knowledge of regulatory requirements and collaborate with international teams.

Skills & Requirements

Must-have

  • Scientific degree required
  • MDR regulation knowledge
  • Analytical and detail-oriented
  • Strong written communication skills
  • Advanced Excel proficiency

Nice-to-have

  • Interest in high-risk devices
  • Basic Spanish language skills
  • International marketing collaboration
  • Methodical approach to tasks

Key Requirements

  • Degree in scientific disciplines
  • Knowledge of MDR regulations
  • Good English proficiency

Work Rights

Not specified

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