Date de publication Type de poste Lieu de travail Expérience Étude Disponibilité Langues Mobilité
9 septembre 2022 CDI Paris, France, France Entre 2 et 5 ans Bac + 5 1500 – 1900 DT / Mois Plein temps Français , Anglais
Description de l’annonce:

In the context of a new project for one of our top Pharma clients, we’re looking for a talented consultant to lead the following missions, and much more!

Responsibilities:

  • Compile, or supervise the compilation of regulatory dossiers in accordance with national requirements
  • Gain regulatory authority approval
  • Provide ongoing regulatory advice to project teams to ensure regulatory concerns are planned and accounted for and the relevant data are generated to meet project objectives
  • Provide regulatory support to clients and associate companies
  • Liaise with external regulatory authorities as required
  • Provide format and contents review of packaging texts, Summary of Product Characteristics, Patient Information Leaflets and labeling
  • Review tasks for, support, and mentor Regulatory Affairs Associates

Profile:

  • Degree in Life Science/ Pharmacy degree would be a plus
  • First experience in Regulatory Affairs in the Pharmaceutical industry
  • Knowledge of Africa and/or MENA regulations for pharmaceuticals (NCE, Biologicals, and Biotech)
  • Excellent communication skills in English, French, and Arabic
  • Excellent attention to detail
  • Ability to work well within a multicultural team
  • Good time management skills

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