DEMO S.A. Pharmaceutical Industry
quality assurance validation supervisor
Oct 7, 2026 · DEMO S.A. Pharmaceutical Industry
Τρίπολη·Oct 7, 2026
ΤρίποληOn SiteΒιομηχανική ΠαραγωγήPermanentFull Time
JOBILY AI SUMMARY
What you'll do
- Lead and develop the Validation team including resource planning, training, and competence development
- Own and manage the site Validation Master Plan, schedule, and calibration/re-qualification plans
- Approve URS, risk assessments, and validation protocols and reports (DQ/IQ/OQ/PQ) ensuring lifecycle PV alignment
- Oversee FAT/SAT execution, manage discrepancy and deviation closeout, change control, and audit readiness
- Lead risk management per ICH Q9, chair risk reviews, and drive risk-based decision making
- Govern CSV/CSA for GxP computerized systems in compliance with Annex 11 and GAMP 5
- Lead Annex 1 compliance for sterile operations including contamination control strategy and aseptic risk controls
- Collaborate cross-functionally with Production, Engineering, QC/QA to ensure project compliance and timeliness
Key requirements
- 5+ years' experience
- Knowledge of EU GMP Annex 15, Annex 11 and FDA 21 CFR 210/211 and Part 11
- Leadership and project management skills with stakeholder communication expertise
- Validation Master Plan management and validation protocols (DQ/IQ/OQ/PQ)
- Risk management per ICH Q9 processes
- CSV/CSA for GxP computerized systems and Annex 1 compliance
- MS Office proficiency and fluency in Greek and English
- Engineering / Scientific field / Business Administrationpreferred
Benefits
- The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment.
About the job
DEMO SA is one of Europe’s leading pharmaceutical manufacturers. We are expanding with new state-of-the-art manufacturing facilities in Tripoli, Arcadia. All roles below are full-time, on-site (day shift) at the new plant, with occasional trips to Kryoneri for training. About the role As a…



