Regulatory Affairs Specialist Role
This role has a significant impact on the preparation and submission of regulatory dossiers to European health authorities.
* The preparation of regulatory dossiers, including registrations, renewals, and variations.
* The organization of dossier submissions to European health authorities.
* Support in drafting administrative and quality variation dossiers.
* Collaboration with the operational team for electronic publication and submission.
This position requires an individual with a post-secondary degree and relevant experience in a similar role. The ideal candidate will possess strong relational skills, excellent organizational abilities, and a commitment to delivering high-quality results.
The successful candidate will have a deep understanding of regulatory affairs principles and practices, as well as exceptional communication and interpersonal skills. They will be able to work effectively in a team environment, manage multiple priorities, and maintain accurate records.
We are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team. If you have a passion for regulatory affairs and a strong desire to deliver exceptional results, we encourage you to apply.