Brussels Metropolitan Area
- Responsible for local operational aspects of RA submission and QA compliance of distribution of products and services - Define Regulatory strategy of the products and implementation of the Quality Management System at country level - Manage regulatory activities relating to specific portfolio of products/projects in Benelux - Act as back-up Responsible Person (RP) for the NL local entity
- Responsible for local regulatory submissions - Design and definition of the regulatory strategy for drugs - Manage RA activities for specific product portfolio/projects (commercialization status, labeling, ..
- Responsible for complex regulatory strategies in support of drug licensing - Consultant to managers - Represent local RA in EMEA and global working groups