* The CQV Engineer will be involved in all validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others
* The validation documentation deliverables include URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ). Prepare validation documents
* Execution of IQ/OQ and PQ for equipment, systems and utilities
* Write reports of completed validation activities
* Work to identify efficiencies in the validation program approach
* Work to apply lessons learned and stay informed of industry regulatory changes as it applies to equipment / facility validation
* Perform assigned Quality Systems activities including Document Management system, Change Control, Non-Conformities, and CAPA’s. Writing and/or revising procedures applicable to the Engineering activities
* Support the Engineering group to prepare the validation, requalification, and maintenance program
* Perform other duties as assigned
* Bachelor’s Degree in Science or Technical field
* English (C1)
* Work Experience: Advanced Level Pharma Industry
* Excellent technical writing skills and the ability to document all work in a thorough, accurate and timely manner
* Excellent written and oral communication skills and the ability to work interdepartmentally in an effective manner to carry out daily duties
* Excellent organizational and time management skills
* Further training opportunities
* Friendly working enviroment
* Renowned Pharma company
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