Regulatory Affairs Manager

Location: Brussels, Belgium (Hybrid; 2-3 days onsite per week)

The Company

We are partnered with one of the largest multi-national consumer goods companies, renowned for it’s extensive range of over-the-counter (OTC) health products, food supplements and medical devices.

The Role

As a Regulatory Affairs Manager, you’ll be part of the Benelux team working towards ensuring that all products (OTC, Food Supplements, Medical Devices) meet regulatory requirements and are brought to market successfully. Your responsibilities will span across regulatory activities, strategy development, compliance maintenance, and organizational advising.

Main Responsibilities:

• Oversee regulatory processes for obtaining product approvals in the Benelux region.
• Create and implement effective regulatory strategies for product submissions.
• Ensure product artwork and advertising materials meet regulatory standards.
• Track local regulatory changes and advise on compliance risks.
• Serve as the primary contact for local health authorities and trade associations.
• Manage budget estimates, expenses, and pricing applications.
• Work with Quality Assurance on audits and corrective actions.
• Coordinate and oversee external regulatory consultants.

Requirements:

• Degree in Pharmacy, or other health related science
• 1-2 years experience in Regulatory Affairs (Medicinal or Non-Medicinal)
• Managed regulatory affairs needed to obtain Marketing Authorizations (MAs) and other authorizations within the Benelux region
• Fluent in Dutch/Flemish and English (written and spoken)

How to Apply

Apply here for a confidential call about this opportunity.