DEMO S.A. Pharmaceutical Industry
regulatory affairs professionals
Oct 7, 2026 · DEMO S.A. Pharmaceutical Industry
Κρυονέρι·Oct 7, 2026
ΚρυονέριOn SiteΔιοίκηση ΕπιχειρήσεωνPermanentFull Time
JOBILY AI SUMMARY
What you'll do
- Lead, coordinate, or support regulatory activities for new submissions, variations, renewals, and lifecycle management
- Prepare, review, compile, and submit high-quality regulatory documentation
- Manage regulatory submissions through DCP, MRP, and National procedures ensuring quality and timeliness
- Act as liaison with Regulatory Authorities and coordinate responses to questions or deficiencies
- Drive cross-functional collaboration for dossier compilation with internal and external partners
- Support regulatory strategy development for assigned products, markets, or projects
- Monitor and manage post-approval regulatory activities including renewals and regulatory updates
- Review regulatory documentation and scientific responses for accuracy and compliance
- Guide, coach, and develop team members and ensure timely delivery of regulatory projects
Key requirements
- Regulatory Affairs expertise in pre-approval and post-approval operations
- Preparation and management of marketing authorization submissions
- Management of regulatory submissions via DCP, MRP, and National procedures
- Regulatory documentation preparation and review
- Knowledge of regulatory requirements and guidelines
- Communication skills and stakeholder management
- Organizational skills and ability to manage multiple priorities
- Fluency in English and MS Office proficiency
- Chemistry / Biology / Pharmacy / Life Sciencespreferred
Benefits
- The company offers competitive salary and benefits, continuous specialized training, career development and a friendly working environment.
About the job
At DEMO S.A., one of the world’s leading pharmaceutical manufacturers in injectable facilities, we are looking for experienced Regulatory Affairs Professionals to join our team. We welcome Senior Professional profiles with expertise in either or both of the following areas: pre-approval operations…



