Regulatory Affairs Specialist - Gdańsk

Join Polpharma as a Regulatory Affairs Specialist and play a key role in ensuring regulatory compliance and lifecycle management of pharmaceutical products across international markets. In this position, you will contribute to the preparation, submission, and maintenance of regulatory dossiers, collaborating in a dynamic, multinational environment and supporting the successful registration of products worldwide. Your responsibilities: Prepare, review, and submit regulatory dossiers (eCTD) for M… Zobacz pełną ofertę