Professional Regulatory Affairs
Vue: 130
Jour de mise à jour: 26-11-2025
Localisation: Nazareth East Flanders
Catégorie: Santé / soins médicaux
Industrie: Research Services Manufacturing Pharmaceutical Manufacturing
Niveau: Associate
Type d’emploi: Full-time
le contenu du travail
Perrigo Company is dedicated to making lives better by bringing Quality, Affordable Self-care products that consumers trust everywhere they are sold. Help us do it.Description OverviewPerrigo Belgium is an organization with a dynamic, transparent and fast-paced atmosphere, characterized by an entrepreneurial and cooperative culture. Regulatory compliance and quality of our products and activities are key in our success; requiring proactive and engaged regulatory professionals.In our Belgian Regulatory Affairs team we are looking for an enthusiastic Regulatory Affairs Professional who will be mainly focused on OTC Medicines and Medical Devices distributed in Belgian & Luxembourg market. The function is part of the Perrigo Benelux & Green Division (BNLG) Regulatory Quality Safety (RQS) cluster team, reporting to the Head of RQS BNLG and with a senior team member acting as mentor. The work location is Nazareth, Belgium (future location will be Ghent as of Q2 2024) (including the flexibility to work from home).Scope of the RoleAs Regulatory Affairs Professional you will have a diverse, challenging role in which you will:- Ensure all Medicinal and Medical Device dossiers you have in your portfolio are launched and maintained compliant to EU and National regulations and in line with business goals
- You will be highly involved in the products’ lifecycle, including New Product Development (NPD) and launches, lifecycle maintenance and promotional activities
- Ensure timely and effective communication and collaboration with other departments including marketing, CSI (trade marketing), sales and corporate regulatory and innovation
- Support the development and clearance of promotional and packaging materials
- Liaise with external stakeholders (e.g. Industry associations)
- Gather and interpret regulatory intelligence and anticipate on emerging chances in legislation and policy
- Analyse regulatory issues incl. impact assessments of changes in regulatory requirements, advise on local implementation strategies and inform relevant stakeholders.
- Participate in regulatory projects.
- Master’s degree in sciences (e.g. Pharmacist, Biomedical Sciences, etc.)
- Minimum 4 years of experience in a pharmaceutical regulatory environment (submission of variations & promotional materials to FAGG)
- Knowledge of pharmaceutical law and regulations
- Recognized as Person Responsible for Information & Publicity (RIP) in Belgium is an asset
- Background knowledge of other types of consumer healthcare products, food supplements or cosmetics is an asset
- The ability to work both autonomously and in teams
- Strong communication, persuasion and problem solving skills
- An eager and quick learner
- Fluent in Dutch and English; knowledge of French; German is an advantage.
- Perrigo Belgium offers you a challenging position within a strong and dynamic company
- A professional environment offering you the opportunity to boost your career through training, coaching & support, learning on the job
- A competitive compensations and benefits package for the required level and experience
- The opportunity to work in a hybrid working model as part of our selfcare and wellbeing strategy. Hybrid working combines caution and flexibility with passion and energy to make our vision a reality.
Date limite: 10-01-2026
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