Regulatory Affairs Specialist

Thema is a fast-growing Italian company of the Complife Group that deals with strategic consultancy in the field of Quality&Regulatory Affairs within the medical sector, specifically in the field of Medical Devices and In Vitro Diagnostic Devices.
For the Regulatory Affairs Specialist position, we are looking for a recent graduate to join the company’s operations team.

What the Regulatory Affairs Specialist does at Thema

Within the function and under the direct responsibility of the Operations Director, they will:

  • Execute assigned tasks and project/job operational activities;
  • Operate for the implementation of the activities/tasks within the scheduled deadlines.

The person we are looking for

The ideal candidate meets the following requirements

  • Bachelor’s degree in a scientific field, preferably with respect to Biomedical Engineering, Management Engineering, Electronic Engineering, Biotechnology, Pharmacy;
  • Good knowledge of the English language;
  • Excellent knowledge of the Microsoft Office package;
  • Interpersonal skills;
  • Excellent ability to work in a team;
  • Personal planning skills.

Direct experience in regulatory affairs in the medical field is not required;

Join us and apply for the position of Regulatory Affairs Specialist!

Find out more about us:

To apply, send your CV to or fill in the application form in just a few clicks and send us your CV in PDF format! Please specify in the subject line “Application for Regulatory Affairs Specialist”.

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