Validation Officer – Quality Assurance

About the role

We are seeking a motivated and detail‑oriented Validation Officer to join our Quality Assurance team at our Schimatari site. The role provides quality oversight for manufacturing processes, facilities, utilities, equipment, and computerized systems, ensuring compliance with EU GMP requirements and internal quality standards.

Key responsibilities

• Support qualification and validation activities for equipment, utilities, facilities, cleanrooms, and computerized systems.
• Review and approve validation documentation, including risk assessments, protocols, and reports.
• Participate in process validation, cleaning validation, and continued process verification.
• Manage deviations, non‑conformances, investigations, CAPAs, and change controls.
• Conduct quality risk assessments and support continuous improvement initiatives.
• Act as QA representative in engineering projects, facility modifications, and new product introductions.
• Support internal, supplier, regulatory, and customer audits.

Required profile

• Bachelor's degree in Engineering, Pharmaceutical Sciences, Chemistry, Biology or related scientific field.
• 2‑5 years experience in a GMP‑regulated pharmaceutical environment.
• Knowledge of EU GMP requirements, Annex 1, Annex 15, Change Control, CAPA and Risk Management principles.
• Fluent in Greek and English, both written and spoken.

Required skills

• EU GMP compliance
• Annex 1
• Annex 15
• Change Control
• CAPA
• Risk Management

What we offer

• Competitive salary and benefits package.
• Free company bus service and private insurance.