DEMO S.A. Pharmaceutical Industry
validation manager
Oct 7, 2026 · DEMO S.A. Pharmaceutical Industry
Κρυονέρι·Oct 7, 2026
ΚρυονέριOn SiteΒιομηχανική ΠαραγωγήPermanentFull Time
JOBILY AI SUMMARY
What you'll do
- Lead and coordinate validation activities for new pharmaceutical manufacturing facilities, utilities, equipment, and computerized systems
- Ensure qualification and validation activities comply with cGMP, FDA, EU GMP, and internal quality standards
- Review and approve validation documentation such as Validation Master Plans, risk assessments, qualification protocols, and validation reports
- Collaborate with Engineering, Projects, Production, Maintenance, Automation, and Quality teams during design, construction, commissioning, qualification, and startup phases
- Maintain validated state of facilities, equipment, utilities, and computerized systems throughout their lifecycle
- Monitor and maintain validation and calibration programs for critical systems and equipment
- Support investigations, deviations, CAPAs, change controls, and requalification activities related to validation
- Participate in regulatory inspections, customer audits, and internal audits providing validation expertise
- Lead, coach, and develop Validation team members promoting quality, compliance, and continuous improvement
- Support cross-functional projects involving facility expansions, equipment installations, technology transfers, and process improvements
Key requirements
- 6+ years' experience
- Qualification and validation of pharmaceutical facilities, utilities, production equipment, and computerized systems
- Validation lifecycle activities including DQ, IQ, OQ, PQ, requalification, and calibration programs
- Good understanding of EU GMP, Annex 1, FDA regulations, 21 CFR Part 11, and Data Integrity requirements
- Project management, planning, and stakeholder management skills
- Leading, coaching, and developing Validation team members
- Experience with commissioning, startup, expansion, and greenfield pharmaceutical projects
- Review and approval of validation documentation including VMPs, risk assessments, qualification protocols, and validation reports
- Collaboration with Engineering, Projects, Production, Maintenance, Automation, and Quality teams
- Handling investigations, deviations, CAPAs, change controls, and requalification activities
- Strong analytical thinking and problem-solving
- Excellent communication skills in Greek and English
- Ability to manage multiple priorities in a fast-paced manufacturing and project environment
- Life Sciences / Engineeringpreferred
Benefits
- The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging 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 candidate for the position of Validation Manager for New Facilities Department. The position reports to the Senior Validation Manager and is based in Kryoneri.…



