DEMO S.A. Pharmaceutical Industry
regulatory affairs - europe (pre-approval) supervisor
Oct 7, 2026 · DEMO S.A. Pharmaceutical Industry
Κρυονέρι·Oct 7, 2026
ΚρυονέριOn SiteΔιοίκηση ΕπιχειρήσεωνPermanentFull Time
JOBILY AI SUMMARY
What you'll do
- Lead EU pre-approval regulatory strategy and documentation requirements
- Own end-to-end dossiers for DCP/MRP/National submissions ensuring quality and timely delivery
- Line-manage and coach Regulatory Affairs Officers and Associates; review and approve key deliverables
- Act as primary liaison with EU Regulatory Authorities and coordinate responses to questions and deficiencies
- Drive cross-functional input for dossier compilation and maintain compliance for registered portfolio
- Ensure policies and procedures are understood, evaluated, and implemented with necessary modifications
- Liaise with various departments to collect required information and documentation for dossier submission and product registration
- Support internal Regulatory department activities to ensure compliance of registered products
- Compile and monitor scientific responses to deficiencies raised by Regulatory authorities
Key requirements
- 5+ years' experience
- Regulatory strategy with knowledge of EU regulatory guidelines and dossier preparation for DCP/MRP/National submissions
- Line management and coaching with effective communication and relationship management skills
- Liaison with EU Regulatory Authorities and cross-functional coordination
- Policy and procedure understanding with ability to work under pressure and resilience
- MS Office skills with strong organizational and multitasking abilities
- Fluent English
- Pharmacy / Biology
Benefits
- The company offers competitive salary and benefits, continuous specialized training, career development and a friendly working environment.
About the job
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…



