Position Details

Job Overview:
The Regulatory Affairs Manager will be responsible for overseeing the registration, renewal, and ongoing regulatory compliance of veterinary medicinal products and feed additives within the European Union (EU). This role requires a deep understanding of EU regulatory frameworks and the ability to navigate the complex landscape of veterinary product registrations and renewals. The Regulatory Affairs Manager will work with cross-functional teams, leverage the use of external regulatory consultants and liaise with regulatory authorities, and ensure that all products comply with applicable EU laws and guidelines. In addition to regulatory oversight, the Regulatory Affairs Manager will act as the representative for the Wholesaler’s Dealers Authorization (WDA) for the organization, ensuring compliance with all relevant whole distribution regulations.
The Regulatory Affairs Manager will support the region for:
All regulatory requests /inquiries from the authorities and/or customers. 
Regulatory support as required by manufacturing site in the region and /or CMO’s 
Training all EU employees on best practices and EUGXP compliance. 
The regulatory affairs manager would be eligible to be the responsible person (RP) for the distribution of veterinary products from our distribution center in Belgium.