About this role
Regulatory Affairs CMC Manager – Dossierprüfung & Lifecycle Management (m/w/d) at ROTOP Pharmaka GmbH. Location: Dresden, Saxony, Germany. Role: reviewing dossiers, managing lifecycle, coordinating projects Requirements: Scientific degree required; some professional experience in regulatory affairs; CMC knowledge and CTD (Module 3) experience preferred; strong communication and organizational skills; German and English proficiency. Category: Legal and Compliance Seniority: Mid Level Commitment: Full Time, Part Time Workplace: Onsite Languages: German, English