Validation Engineer | Equipment & Process Qualification – Vilnius
Core
Ensure equipment, systems, facilities, and processes are properly qualified, compliant, and ready for reliable operations in manufacturing and laboratory environments.
Role type
Validation Engineer (Equipment & Process Qualification)
Builds
Qualified state of production and laboratory equipment and processes for life science and diagnostic technologies
Domain
Life sciences, diagnostics, pharmaceutical manufacturing, regulated technical environments
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Equipment qualification, process validation, IQ/OQ/PQ protocols, GMP compliance, deviation investigation, CAPA implementation, risk assessment, technical writing, regulatory knowledge (FDA/ISO/GAMP5), cleanroom operations
Preferred skills
Production/laboratory/utility system qualification, quality management systems, statistical analysis, process control methods, contractor coordination
Technologies
Microsoft Office tools
Responsibilities
Plan and execute qualification activities for equipment and processes; Prepare and review validation documentation (IQ/OQ/PQ); Investigate deviations and implement corrective actions; Coordinate technicians and external specialists; Support process improvements related to validation compliance
Seniority
Mid-level, hands-on IC
