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Pharma - Regulatory Affairs & Responsible for Information (RIP)

Brussels Permanent View Job Description
Our client is seeking a Regulatory Affairs Officer & Responsible for Information (RIP) to join the Pharmaceutical Team in Brussels. The ideal candidate has a master in Pharma, +3 years of experiences in Regulatory Affairs, a RIP number and is French speaking.

Added 24/03/2026

  • Manufacturing Pharma Industry - OTC, Cosmetics & Food Supplements
  • Healthcare - Regulatory affairs officer - Responsible for Information (RIP)

About Our Client

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.

Job Description

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.

The Successful Applicant

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.



What's on Offer

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

  • An attractive salary package, including company car, net allowances, insurances, meal & eco vouchers, and compensatory leave days.
  • Flexible working arrangements for a better work-life balance.
  • Training opportunities and a supportive, human‑centered work environment within a passionate and innovative team.



Contact
Morgane Delgeye
Quote job ref
JN-032026-6974925

Job summary

Sector
Life Sciences
Sub Sector
Regulatory Affairs
Industry
Industrial / Manufacturing
Location
Brussels
Contract Type
Permanent
Consultant name
Morgane Delgeye
Job Reference
JN-032026-6974925

PageGroup is an equal opportunity employer committed to workforce diversity, both as an employer as well as a recruitment service provider. Each recruitment decision we make for people we hire and people we place into new roles is based solely on the candidates’ knowledge, experience and skills.