Drug Regulatory Affairs Associate EU (m/f)

Our client, a pharmaceutical company in Munich, is currently looking for a

Drug Regulatory Affairs Associate EU (m/f)

Activities and responsibilities

  • Verification, preparation and submission of variation and renewal documentation for European market authorizations
  • Administrative and specialist support of molecule manager for complex variations
  • Maintenance of regulatory data and documentation in corresponding databases
  • Communication with European health authorities (English and German)
  • Self-reliant variation planning and tracking

Qualification profile

  • M.Sc. or Diploma in sciences (biology, chemistry, biochemistry, pharmaceutical sciences) with at least 2 years of experience in pharmaceutical industry
  • Experience in drug regulatory affairs of advantage
  • Very good organizing abilities and time management
  • High communication skills, team player and ability to work under pressure
  • Good knowledge of MS Office, SAP and IT affinity
  • Fluent in English and German


  • Fascinating employer
  • Access to non- published job offers
  • Active presentation of your qualifications to our client
  • Advise on your application from our recruitment specialists
  • Representation and Protection of your interest

Send application to

Deborah Angelè
Kelly Services München
T: 089 3840907
M: deborah.angele[at]kellyservices.de

While applying for the job please refer to jobvector

About Kelly Scientific Resources München

Unsere Berater und Manager im Fachbereich Kelly Scientific Resources - alle ebenfalls ausgebildete Naturwissenschaftler mit langjähriger Berufserfahrung - widmen sich mit ihrer Fachkenntnis ausschließlich der Identifizierung, Beratung und Vermittlung von naturwissenschaftlichem und medizinischem Fach- und Führungspersonal in einem breiten Spektrum von Branchen und Berufsfeldern. Wir erkennen...

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