Senior Regulatory Affairs Manager – EuropeA European‑focused regulatory role supporting the development, registration, and lifecycle management of speciality, orphan, paediatric, and generic medicines.Key ResponsibilitiesDevelop and execute EU regulatory strategies for innovative, speciality, and complex products.Review non‑clinical and clinical data packages and identify gaps for regulatory submissions.Lead/assist with MAAs, variations, line extensions, renewals, and post‑approval commitments.S