Cleaning Validation Engineer

Initiating and leading process and systemic improvements. Solving technological problems in production processes. Leading investigations (Deviation / OOS / Complaints) and implementing Corrective and Preventive Actions (CAPA). Writing technological documents and validation documents in English and working on the production floor. Routine work with interfaces: Production, Quality Assurance, Quality Control, Development, Regulatory, and Engineering. Updating and writing procedures. Working in a dynamic environment. Managing validation status for all products.

At least a Bachelor's degree in Chemical Engineering, Biotechnology, Pharmacy, or Life Sciences - mandatory. Experience as a Validation Engineer - advantage. Proficiency in working in a GMP environment - advantage. Very high level of English – including fluent technical writing. Willingness to work overtime if necessary. Precision, order, and organization. Advantages:

Ability in project management, working with many interfaces, and systemic vision. Proactive approach, analytical thinking, and independent problem-solving ability. Familiarity with improvement methodologies. Experience working with systems such as SAP, TrackWise.