Quality Assurance Validation Supervisor
Demo S.A.Tripoli, Peloponnese, Western Greece and the Ionian, Greece • Municipal Unit of Sikyona, Peloponnese, Western Greece and the Ionian, Greece
Posted October 13, 2025
Full Time
About the Company
DEMO is a dynamic Greek industrial and commercial organization, specializing in the development, production and supply of pharmaceutical products. The company is the largest supplier of injectables for public hospitals in Greece, exports 80% of its annual production and is recognized as one of the official suppliers of the United Nations, UNICEF, the World Health Organization (WHO), Doctors Without Borders and the International Committee of the Red Cross. With over 3,300 circulation licenses in 86 countries worldwide, the largest factory in SE Europe and over 1,400 employees, DEMO paves the way for pharmaceutical self-sufficiency for Greece and Europe. Today, DEMO implements investments of €356 million, strengthening production and R&D, while entering the development and production of active ingredients and Biotechnology. At the same time, the company is committed to ensuring equality, diversity and inclusion in the working environment and has adopted -within this context- the Diversity Charter for Greece. DEMO moves "Always Forward" driven by its corporate philosophy of providing quality and reliable pharmaceutical products, for everyone. Learn more at www.demo.gr
Job Description
DEMO SA, a leading European pharmaceutical manufacturer, is expanding with new manufacturing facilities in Tripoli, Greece. The role is for a Validation Supervisor responsible for leading the site Validation program across various areas, ensuring compliance with Annex 1/15/11 regulations and establishing a robust Contamination Control Strategy. This position involves project leadership, risk assessment, and cross-functional collaboration.
Requirements
- BSc in Engineering or related scientific field
- More than 5 years in pharmaceutical validation (including sterile/aseptic), with ≥2 years in a supervisory/lead role
- Deep knowledge of EU GMP Annex 15/11/1, FDA 21 CFR 210/211 & Part 11
- Fluency in Greek and English
- Proficiency with MS Office
Benefits
- Competitive remuneration
- Continuous learning and development opportunities
- Friendly and challenging working environment