Validation Supervisor
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Before you apply
LocationTripoli, Peloponnese Region, Greece
Work modeon-site
Typefull-time
SeniorityLead
Experience5+ yrs
DepartmentQuality Assurance
Company size501–1,000 people
PostedOct 13, 2025 · 1y ago
Verified live6h ago
May no longer be actively hiring
Posted by the company on Oct 13, 2025
At a glanceSummarised by Seekless from the posting.
BSc in Engineering or related scientific field
More than 5 years in pharmaceutical validation (including sterile/aseptic)
≥2 years in a supervisory/lead role
Deep knowledge of EU GMP Annex 15/11/1, FDA 21 CFR 210/211 & Part 11
Strong understanding of lifecycle PV (PPQ/CPV)
Proven leadership
Proven project management
Stakeholder communication skills
Fluency in Greek
Fluency in English
Proficiency with MS Office
MSc or MBA is a strong plus
Skills
MS Office
About the company
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 Validation Supervisor, you will lead the site Validation program across equipment, utilities, cleanrooms and processes, ensuring Annex 1/15/11 compliance and governing the site Contamination Control Strategy (CCS) and Validation Master Plan (VMP).
Responsibilities
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Lead and develop the Validation team; plan resources, training and competence development.
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Own the site VMP, validation schedule and re‑qualification/calibration plans; monitor KPIs and report to senior management.
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Approve URS, risk assessments and DQ/IQ/OQ/PQ protocols and reports; ensure alignment with lifecycle PV (PPQ/CPV).
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Oversee FAT/SAT execution, discrepancy/deviation closeout, change control and audit/inspection readiness.
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Ensure robust QRM practices per ICH Q9 (R1); chair risk reviews and drive risk‑based decision making and subjectivity controls.
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Govern CSV/CSA approach for GxP computerised systems in line with EU Annex 11 and GAMP 5 (Second Edition).
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For sterile operations: lead Annex 1 compliance (CCS, EM strategy and trending, barrier technologies, aseptic risk controls).
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Cross‑functional collaboration with Production, Engineering, QC/QA to ensure timely, compliant project execution.
Employment Type
Permanent, on-site (day shift) at DEMO SA’s new manufacturing plant in Tripoli, Arcadia. Occasional trips to Kryoneri for training.
Requirements
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BSc in Engineering or related scientific field; MSc or MBA is a strong plus.
•
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; strong understanding of lifecycle PV (PPQ/CPV).
•
Proven leadership, project management and stakeholder communication skills.
•
Fluency in Greek and English; proficiency with MS Office.
Benefits
The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment.