About this role
Expert Regulatory Affairs at Recipharm (Wasserburger Arzneimittelwerk GmbH). Location: Wasserburg am Inn, Bavaria, Germany. Role: preparing documentation, assessing risks, responding inquiries Requirements: Scientific degree required; 2+ years regulatory/marketing authorization experience with CMC/CTD (Module 3), ability to prepare registration dossiers, perform risk assessments (toxicology), and respond to client and authority inquiries. Category: Legal and Compliance Seniority: Mid Level Certifications: mdra Commitment: Full Time Workplace: Onsite Languages: German, English