Regulatory Affairs consultant - health animal
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).
Requirements
Education : Qualified Pharmacist or a Master’s degree