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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.…

DEMO S.A. Pharmaceutical Industry
DEMO S.A. Pharmaceutical Industry
Company Profile

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.

Workplace
On Site
Sector
Βιομηχανική Παραγωγή
Employment Type
Permanent
Work Time
Full Time
DEMO S.A. Pharmaceutical Industry
DEMO S.A. Pharmaceutical Industry
Company Profile

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.