DEMO S.A. Pharmaceutical Industry
validation engineer
Oct 7, 2026 · DEMO S.A. Pharmaceutical Industry
Τρίπολη·Oct 7, 2026
ΤρίποληOn SiteΒιομηχανική ΠαραγωγήPermanentFull Time
JOBILY AI SUMMARY
What you'll do
- Issue Quality Risk Management reports on design, qualification, validation, control, and monitoring of new pharmaceutical facilities
- Prepare or review URS and qualification/validation protocols and reports (DQ/IQ/OQ/PQ) ensuring credibility
- Develop, issue, and revise QA procedures (SOPs) for activities in new facilities
- Lead deviation investigations and perform root cause analysis with CAPA follow-up
- Verify compliance of production and support areas with legislation, standards, and internal procedures
- Execute and document FAT/SAT prior to commissioning; support change control and requalification
- Perform equipment, utilities, and cleanroom qualification and temperature mapping
- Conduct formal risk analyses (FMEA/FMECA/FTA/HACCP) and implement mitigation measures
- Support Computerised Systems activities in line with EU Annex 11 and GAMP 5 principles
- Ensure ongoing validated status of equipment/systems and adherence to cGMP and data integrity (ALCOA+)
- Participate in Annex 1 compliant activities including contamination control, EM qualification, and barrier technologies
Key requirements
- 2+ years' experience
- Risk Management Tools including FMEA, FMECA, FTA, HACCP
- Cleaning Validation, Process Validation, and Facility Design
- FDA 21 CFR 210/211 and FDA 21 CFR Part 11 regulatory knowledge
- EU GMP including Annex 15, Annex 11, and Annex 1 standards
- Qualification/Validation Protocols (DQ/IQ/OQ/PQ)
- Quality Risk Management, Deviation Investigations and Root Cause Analysis
- Computerized Systems Validation in compliance with CSV/CSA and GAMP 5
- Data Integrity principles including ALCOA+
- MS Office proficiency
- Engineering / Life Sciences / related disciplinepreferred
Benefits
- The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment.
About the job
As a Validation Engineer, you will ensure compliance and quality across our new sterile pharmaceutical installations in Tripoli, supporting the full CQV lifecycle and contributing to a robust Contamination Control Strategy (CCS). Responsibilities - Issue Quality Risk Management (QRM) reports…



