Para empezar
Oportunidades de empleo
Volver a búsqueda de trabajos

Regulatory Affairs Consultant

  • Ubicación:


  • Contacto:

    Aurore Munaut

  • Tipo de trabajo:


  • Teléfono de contacto:

    +32 10 68 53 31

  • Industrias:

    Pharmaceutical , Life Sciences

  • Correo de contacto:

Are you an experienced Regulatory Affairs Consultant willing to work within a pharmaceutical company specialized in OTC medications, food supplements, cosmetics and other healthcare products ? Apply now to know more about this exciting opportunity !

Job Description

As an Regulatory Affairs Consultant, you carry out all regulatory actions to obtain and maintain licenses/registrations to commercialize products, within the defined timelines and in accordance with the applicable regulations.


  • Preparing, drafting, submitting (possibly in collaboration with external partners) and following up the registration dossiers in accordance with the applicable guidelines.
  • Performing all necessary actions required to maintain the licenses/registrations (variations, renewals, notifications, PSUR, …).
  • Formulate proposals to the RA Manager about the possible approach and planning of the registration procedure.
  • Coordinating the registration procedure in the countries involved, after validation of the working method and planning by the RA Manager.
  • Analysis of the regulatory impact of changes to existing products. This includes changes to the quality part (production, analysis, specifications, APIs/raw materials, etc), as well as the clinical part (indications, side effects, claims, etc) of the dossier.
  • Following the legislation and detailed regulatory and scientific guidelines in the countries concerned for products with different legal statuses.
  • Answer the questions asked for certain products by the relevant authorities, pharmacists, doctors or customers, after internal and/or external consultation and validation by the RA Manager.
  • Prepare impact analysis in response to changes in applicable regulations and formulate proposals and recommendations to ensure compliance.
  • Checking and approving all packaging material and checking (and possibly notifying) advertising and promotional material.


  • Master's degree in a scientific field such as pharmaceutical sciences (pharmacist), drug development, biomedical sciences, bioengineering, (bio)chemistry or similar.
  • Several years of RA experience in a pharmaceutical company, specifically in medicinal - food supplements.
  • You are familiar with the different stages of drug development and production in a pharmaceutical company.
  • You have a good knowledge of the relevant national, European and international legislation, procedural regulations and technical rules for products with different legal statuses.
  • Able to work independently and in an organized manner.
  • Excellent sense of priorities and accuracy
  • Flexible and ability to adapt to changing circumstances/needs.
  • You stay informed of developments in the field.
  • Your speak Dutch and English. French is a plus.
  • Good knowledge of Word, Excel and Outlook
  • You have experience with local authorities in Belgium (FAMHP) & Luxembourg (Ministère de la Santé)
  • The existing right to work in Europe


  • A balanced salary package based on your capabilities and experience
  • 50% presence on-site
  • 6 month's project with extension possible

Vacancy number: 20706