On behalf of our Client who are an International Pharma Group, we are looking for an experienced Regulatory Affairs Specialist to join their team in Spain. In this role you will report to Head of Regulatory Affairs.


  • Preparing EU submissions and submitting regulatory dossiers
  • Setting strategies for European branded generic drug registrations
  • Monitoring, preparing and following-up on renewals for all registered products
  • Maintenance of all files and documentation pertaining to regulatory activities
  • Dealing with queries from regulatory bodies and health agencies

Desired experience:

  • Educational background in life sciences
  • Min. 5 years of experience in regulatory affairs with small molecule drugs (generic or innovative)
  • Preferred experience of working with EMA and good knowledge of regulatory procedures in Europe
  • Fluency in English, Spanish would be an extra asset

In return you can expect an attractive remuneration and interesting international work environment. If you meet the above criteria and are interested, please send your up-to-date CV with contact details to joanna.osiak@pharmaprofessionals.eu

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