Pharma - Regulatory Affairs & Responsible for Information (RIP) M/V/X

Description de l'entreprise

Our client is a French pharmaceutical company specialized in producing cosmetics products, food supplements and homeopathic solutions. With more than 2000 employees around the globe, they are committed in delivering high quality & innovative medicines.

Description de la fonction

As a successful Pharma - Regulatory Affairs & Responsible for Information (RIP)- Brussels - French & Dutch, you will have the following responsibilities:

• Ensuring full regulatory compliance for product portfolio in Belgium and Luxembourg.
• Managing regulatory dossiers for medicines (OTC), medical devices, cosmetics, and food supplements.
• Preparing, submitting, and following up with the authorities (incl. AFMPS) on marketing authorizations, notifications, variations, and post-market obligations.
• Monitoring regulatory changes, interpreting legislation, and ensuring continuous product compliance.
• Coordinating with the headquarters for centralized (EU) dossiers and supporting internal teams (marketing, sales.) on regulatory matters.
• Maintaining regulatory databases and improving internal processes.
• Acting as RIP, ensuring all scientific and promotional material is accurate, objective, and compliant with legal requirements, and approving all communication related to medicines.

Profil

As a successful Pharma - Regulatory Affairs & Responsible for Information (RIP)- Brussels - French & Dutch, you will have the following profile:

• Master Degree in Pharmacy
• + 3 years of experiences in Regulatory Affairs
• An official RIP accreditation
• Competencies including time & project management, organization, rigor, flexibility, stress resistance, and the ability to multitasks
• Excellent communication, negotiation, teamwork, and drafting skills.
• Good command of Office tools and an open, creative mindset.
• Strong language skills: French required, Dutch is a plus.

Compétences linguistiques

• Français (atout)

  • Comprendre : Expérimenté - (C1)
  • Écrire : Expérimenté - (C1)
  • Lire : Expérimenté - (C1)
  • Parler : Expérimenté - (C1)

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