
Regulatory Affairs and Safety Associate Self-Care BNL (Brussels, Brussels-Capital Region, BE, 1000) presso Reckitt
Reckitt · Brussels, Belgio · Onsite
- Professional
- Ufficio in Brussels
We are Reckitt
Research & Development
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
About the role
Working in partnership with Regional & Global Regulatory, driving operational excellence across the teams incorporating new medicinal product legislation/regulation requirements and industry best practices as required. Cooperation with local business and strategy development + execution in order to capture business ambitions.
You will be a key point of contact to Global Regulatory, Regional Regulatory and local Regulatory teams with respect to OTC medicinal products, relaying knowledge about external factors and internal impact on processes and timings, as well as point of contact for local business leaders and commercial teams
Engage with local trade association working groups to align on regulatory topics and coordinate industry feedback to health authorities, ensuring Reckitt’s interests are represented through collective association initiatives.
Your responsibilities
- Act as Back-up Responsible Person ensuring compliance with Good Distribution Practices (GDP) and maintaining the Quality Management System in the RP’s absence.
- Oversee product quality and compliance - including supplier and customer approval, complaint handling, recalls, and disposition of returned or falsified products.
- Ensure an effective quality management system, self-inspections, and implementation of corrective and preventive actions.
- Lead regulatory strategy and submissions for Self-Care/OTC products in the Benelux region in alignment with the Iberia/France/Benelux.
- Collaborate cross-functionally with Marketing, Safety, and Global/Regional Regulatory teams to secure timely approvals for registrations, artworks, and advertising materials.
- Serve as Drug Safety Officer (DSO) ensuring local implementation of EU and national pharmacovigilance legislation.
- Maintain proactive communication with Health Authorities (RMS role for MRP, DCP, and RUP procedures) and support responses to regulatory queries.
- Participate in regulatory intelligence and post-market surveillance, contributing to EU intelligence reviews, PMS meetings, and Annual Management Reviews.
- Influence external stakeholders, including trade associations and government agencies, on legislative and regulatory developments aligned with company interests.
- Foster a culture of compliance and collaboration, building strong relationships with internal partners and ensuring “right first time” regulatory execution.
The experience we're looking for
- 2–6 years of full time experience in Regulatory Affairs or Drug Safety, preferably within OTC (Self-Care) or pharmaceutical (Rx) products.
- Strong understanding of Benelux (BNL) regulatory requirements and local health authority procedures.
- Proven experience with advertising and promotional material submissions, including copy review and approvals.
- Familiarity with Good Distribution Practices (GDP) and quality management principles.
- Experience in pharmacovigilance and post-market surveillance activities.
- Excellent communication and relationship-building skills, with the ability to collaborate across regional and global teams.
- Fluent in English and at least one local language (French or Dutch); proficiency in both is an advantage.