About this role
Director Regulatory Affairs at Hansa Biopharma. Location: Lund, Skåne County, Sweden. Role: leading strategy, preparing submissions, liaising authorities Requirements: MSc in pharmacy/chemistry or similar, 10+ years industry experience and 7+ years in regulatory affairs preferred; experience with regulatory strategies, clinical trial submissions, BLA/MAA, and health authority interactions (FDA/EMA). Strong communication and strategic skills. Category: Research and Development (R&D) Seniority: Senior Level Commitment: Full Time Workplace: Hybrid Languages: English