Validation Engineer | Equipment & Process Qualification – Vilnius
Core
Execute equipment, systems, facilities, and process qualification activities to ensure compliance and reliable operations in a regulated life science manufacturing environment.
Role type
Validation Engineer (Equipment & Process Qualification)
Builds
Qualified equipment, systems, and processes for life science and diagnostic technologies
Domain
Life Sciences / Pharmaceutical Manufacturing / GMP
Required skills
GMP compliance, IQ/OQ/PQ protocols, validation documentation, deviation investigation, CAPA, risk assessment, technical writing, cleanroom operations
Preferred skills
Equipment qualification, process validation, quality management systems, gap analysis, contractor coordination, calibration/metrology
Technologies
Microsoft Office
Responsibilities
Plan and execute qualification activities, maintain validation schedules, prepare and review IQ/OQ/PQ documentation, investigate deviations, define corrective actions, coordinate with cross-functional teams, support process improvements
Seniority
Mid-level, hands-on IC
