QA Engineer
Quality Assurance Validation Engineer
Athens
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At Demo SA, one of the world's largest pharmaceutical manufacturers in injectable facilities, we are looking for a high caliber Quality Assurance Validation Engineer to join our team. This position is based in Athens, Kryoneri. As a Validation Engineer, you will ensure compliance and quality across our sterile pharmaceutical installations, supporting the full CQV lifecycle and contributing to a robust Contamination Control Strategy (CCS).
Responsibilities
- Issue Quality Risk Management (QRM) reports covering design, qualification, validation, control, and on-going monitoring of facilities through the quality system
- Prepare or review URS, qualification/validation protocols and reports (DQ/IQ/OQ/PQ) and related procedures, ensuring credibility commensurate with criticality
- Develop, issue and revise QA procedures (SOPs) for planned activities in the facilities
- Lead deviation investigations across production and CQV activities; perform root cause analysis and ensure effective CAPA follow-up
- Verify that production and support areas meet current Legislation, Standards and Internal Procedures; review and track CAPAs from internal audits
- Execute and document FAT/SAT prior to commissioning; support change control and re‑qualification
- Perform equipment, utilities and cleanroom qualification; execute temperature mapping for controlled areas and storage
- Conduct and document formal risk analyses (e.g., FMEA/FMECA/FTA/HACCP) and implement mitigation measures
- Support Computerised Systems activities in line with EU Annex 11 and GAMP 5 (Second Edition) principles (CSV/CSA) as applicable
- Ensure ongoing validated status of equipment/systems, strict adherence to cGMP and data integrity (ALCOA+)
- For sterile operations: participate in Annex 1-compliant activities (CCS, EM qualification and trending, barrier technologies)
Requirements
- BSc in Engineering, Natural Sciences or related discipline (MSc considered a plus)
- ≥2 years' relevant experience in industrial production; experience in pharmaceutical validation for injectables is preferred
- Hands-on experience with risk management tools (FMEA, FMECA, FTA, HACCP)
- Experience in Cleaning Validation, Process Validation and facility design
- Good understanding of FDA 21 CFR 210/211, 21 CFR Part 11, EU GMP including Annex 15 (Qualification & Validation), Annex 11 (Computerised Systems) and Annex 1 (Sterile)
- Excellent command of Greek and English; strong MS Office skills
- Critical thinking, problem-solving, flexibility; ability to manage multiple priorities and meet manufacturing deadlines
Benefits
The company offers competitive compensation, continuous training & career development opportunities and a friendly working environment.
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