At Demo SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented Regulatory Affairs - Europe (Pre-Approval) Supervisor to join our team. This position is based in Athens, Kryoneri.
Responsibilities:
- Lead EU pre‑approval regulatory strategy and documentation requirements.
- Own end‑to‑end dossiers for DCP/MRP/National submissions, ensuring quality and on‑time delivery.
- Line-manage/coach Regulatory Affairs Officers & Associates; review and sign off key deliverables.