We are redirecting you to the source. If you are not redirected in 3 seconds, please click here.

Regulatory Affairs consultant - health animal at Excelya. Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.. This role is an exciting opportunity to contribute to a dynamic, ambitious team in Regulatory affairs department. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.. Responsibilities : . Reporting to the Registration Department Team Manager, you are responsible for all activities related to the obtention, follow-up and maintenance of Marketing Authorizations (MA) in France and Europe, including:. Submission and follow-up of Marketing Authorization applications at both national and European levels.. Preparation, submission and follow-up of regulatory evaluations with Competent Authorities for: pharmaceutical variations, MA renewals, Requests for Amendments to Product Information (DMI), regulatory variations, up to their practical implementation.. Monitoring product registration in the Generic Groups Directory.. Acting as an interface with internal departments, external experts, API manufacturers and contract manufacturing organizations (CMOs).. Education : Qualified Pharmacist or a Master’s degree . Experience : Solid experience in the field of Regulatory Affairs in Veterinary Medecine. . Skills : You are well-organized and detail-oriented, with excellent interpersonal and writing skills in both French and English. Self-motivated and autonomous, you are able to manage priorities effectively and demonstrate strong analytical and synthesis skills.. Language : operational level of English, with good reading comprehension and written communication abilities.. Company Location: Belgium.