Για εργοδότες
Quality Assurance Validation Supervisor


DEMO AΒΕΕ logo
501-2000
Φαρμακευτικές & Κλάδος Υγείας
πριν 4 ώρες
Ημ. ανάρτησης
πριν 4 ώρες

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

  • Lead and develop the Validation team; plan resources, training and competence development.
  • Own the site VMP, validation schedule and re‑qualification/calibration plans; monitor KPIs and report to senior management.
  • Approve URS, risk assessments and DQ/IQ/OQ/PQ protocols and reports; ensure alignment with lifecycle PV (PPQ/CPV).
  • Oversee FAT/SAT execution, discrepancy/deviation closeout, change control and audit/inspection readiness.
  • Ensure robust QRM practices per ICH Q9 (R1); chair risk reviews and drive risk‑based decision making and subjectivity controls.
  • Govern CSV/CSA approach for GxP computerised systems in line with EU Annex 11 and GAMP 5 (Second Edition).
  • For sterile operations: lead Annex 1 compliance (CCS, EM strategy and trending, barrier technologies, aseptic risk controls).
  • 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

  • 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.

Σχετικά tags
qa
qualityassurance
pharmaceutical
peloponnese
manager
ΠΕΡΙΛΗΨΗ ΘΕΣΗΣ
Quality Assurance Validation Supervisor
DEMO AΒΕΕ logo
Τρίπολη
πριν 4 ώρες
Με μεγάλη εμπειρία
Πλήρης απασχόληση

Quality Assurance Validation Supervisor