Benelux Regulatory Affairs Lead

Perrigo Company plc; Gent; Hybride; EUR 110 000 - 150 000; Plein temps

Avantages offerts par ce poste

Total Rewards program

Hybrid work arrangement (2 days from 1

Flexible, hybrid work options

Résumé du poste

Perrigo Company plc in Belgium invites a Regulatory Affairs Senior Manager Benelux to lead regulatory activities across Belgium, the Netherlands, and Luxembourg. You will serve as the legally designated Responsible Person for Information & Publicity and as Local Contact Person for Vigilance, guiding lifecycle management and health authority interactions.

You will shape regulatory strategy, approve promotional materials, support product launches, and ensure compliance with EU and Benelux

Qualifications

• University degree in Pharmacy or Life Sciences required.
• Pharmacist qualification preferred.
• Eligible to act as Responsible Person for Information & Publicity in Belgium and Local Contact Person for Vigilance in Benelux.
• Minimum 6 years of Regulatory Affairs experience with leadership experience.

Responsabilités

• Lead Regulatory Affairs activities across Belgium, the Netherlands, and Luxembourg.
• Oversee the preparation, submission, approval, maintenance, and lifecycle management of regulatory dossiers, permits, licenses, certificates, authorizations, and notifications.
• Provide strategic regulatory guidance to support new product introductions, lifecycle management, labeling updates, and market expansion initiatives.
• Monitor changes in the regulatory environment and advise management on regulations, risks, and opportunities.
• Support business continuity by ensuring regulatory compliance throughout all activities.

Connaissances

English (Fluent)

Dutch (Fluent)

French (Desirable)

German (Asset)

Formation

Master's degree in Pharmacy or Life Sciences

Pharmacist qualification preferred

Description du poste

Perrigo Company plc in Belgium invites a Regulatory Affairs Senior Manager Benelux to lead regulatory activities across Belgium, the Netherlands, and Luxembourg. You will serve as the legally designated Responsible Person for Information & Publicity and as Local Contact Person for Vigilance, guiding lifecycle management and health authority interactions.

You will shape regulatory strategy, approve promotional materials, support product launches, and ensure compliance with EU and Benelux